Biofield Pharma Private Limited

PLEXOCID is a dental gel containing:

• Potassium Nitrate 5% – Helps reduce tooth sensitivity by calming nerve endings in the dentin

• Sodium Monofluorophosphate 0.70% – Provides fluoride for strengthening enamel and preventing dental caries

• Triclosan 0.30% – An antimicrobial agent that reduces plaque formation and helps prevent gingivitis

It is commonly used for sensitive teeth, early dental caries, and mild gum inflammation.

1. Potassium Nitrate: Diffuses into dentinal tubules and reduces excitability of nerve fibers, decreasing sensitivity to cold, heat, or sweet stimuli.

2. Sodium Monofluorophosphate: Enhances enamel remineralization and protects against acid attack from bacteria.

3. Triclosan: Inhibits bacterial growth in the oral cavity, reducing plaque and inflammation.

• Dentinal hypersensitivity (sensitive teeth)

• Prevention of dental caries

• Plaque control and mild gingivitis

• Apply a pea-sized amount directly to affected teeth using a clean finger or soft toothbrush

• Leave on for a few minutes; avoid rinsing immediately for maximum effect

• Use once or twice daily, or as directed by a dentist

• Avoid swallowing the gel

• Not recommended for children under 12 unless advised by a dentist

• Use caution in patients allergic to any of the components

• Prolonged use should be monitored to prevent fluoride overexposure

• Mild temporary tooth or gum irritation

• Rarely, slight taste alteration

• Multi-action gel: desensitizes teeth, strengthens enamel, and controls plaque

• Safe for daily dental care when used as directed

• Provides targeted relief for sensitive teeth

Additional Information:

• Production Capacity: Fully automated, ISO & USFDA-compliant 600,000 Sq. ft. plant with zero liquid & gas discharge facility
• Delivery Time: 45-60 DAYS
• Packaging Details: Our packaging is designed to ensure maximum product safety, stability, and market appeal. We utilize high-quality raw materials (RM) and USFDA-approved packaging components, making our products ideal for export and third-party manufacturing. Key Features of Our Packaging: ✅ Attractive & Market-Differentiating Designs: Our products come with customizable branding and change parts, allowing businesses to create a distinct identity in the pharma market. ✅ Pharmaceutical-Grade Materials: We use high-density PET bottles, tamper-evident caps, and premium blister foils to maintain product integrity. ✅ Advanced Protection: Our packaging is moisture-resistant, UV-protected, and oxidation-resistant, ensuring longer shelf life and stability. ✅ High-Precision Batch Coding & Labeling: We use laser batch coding, holographic labels, and serialized QR codes for authenticity and traceability. ✅ International Standards for Export: All our packaging materials meet USFDA, EUGMP, and WHO-GMP regulations, ensuring global compliance. Our packaging solutions help PCD Pharma companies, third-party manufacturers, and exporters differentiate their products in highly competitive markets while maintaining the highest pharmaceutical standards.

OSTANU-CCM is an advanced bone-strengthening formulation containing Calcium Citrate Malate (CCM) + Vitamin D3 + Magnesium + Zinc, designed to support superior calcium absorption, improve bone density, and enhance overall skeletal health. It is widely recommended for osteoporosis, osteopenia, fracture recovery, and calcium deficiency conditions.

With its highly bioavailable Calcium Citrate Malate form, OSTANU-CCM ensures better absorption compared to conventional calcium salts—making it ideal for elderly patients, post-menopausal women, and individuals with low bone mineral density.

Manufactured in a WHO-GMP, USFDA, and EUGMP-certified facility, OSTANU-CCM ensures high purity, optimal stability, and superior patient compliance—making it an excellent choice for PCD Pharma Franchise, third-party manufacturing, and export markets.

Calcium Citrate Malate (CCM):
A highly absorbable form of calcium that strengthens bones, improves bone mineral density, and supports teeth health.

Vitamin D3:
Enhances intestinal calcium absorption and ensures proper calcium deposition in bones.

Magnesium:
Supports bone structure, muscle function, and assists in Vitamin D activation.

Zinc:
Promotes bone tissue growth, improves immunity, and supports faster recovery.

This balanced combination enhances calcium utilization, strengthens bones, and reduces fracture risk.

✅ Superior Calcium Absorption with CCM Technology
✅ Strengthens Bones & Improves Bone Density
✅ Supports Osteoporosis & Post-Menopausal Bone Health
✅ Aids in Fracture Healing & Recovery
✅ Enhances Muscle & Joint Support
✅ Manufactured in WHO-GMP & USFDA-Certified Facilities
✅ EUGMP-Compliant for Regulated Export Markets
✅ PCD Pharma & Third-Party Manufacturing Ready
✅ Premium Blister Packaging for Better Stability & Shelf Life

✔️ Patients with osteoporosis & osteopenia
✔️ Post-menopausal women
✔️ Elderly individuals with bone weakness
✔️ Growing adolescents needing calcium support
✔️ Patients recovering from fractures
✔️ Suitable for wholesalers, stockists & international importers

Mild constipation

Bloating

Nausea

Excessive intake may cause hypercalcemia

(Use under medical supervision.)

✅ DMF-Grade Raw Materials & Quality Excipients
✅ Clinically Advanced CCM-Based Formula
✅ Strict Microbial & Cross-Contamination Control
✅ High Stability & Extended Shelf Life
✅ Export-Quality Manufacturing Standards
✅ Dedicated Technical & After-Sales Support

✔️ PCD Pharma Franchise for Calcium CCM Tablets
✔️ Third-Party Manufacturing of Bone Health Supplements
✔️ WHO-GMP Certified Calcium & Vitamin D3 Manufacturer
✔️ USFDA & EUGMP Approved Orthopedic Products for Export
✔️ Premium Bone & Joint Support Supplements for Distributors

Additional Information:

• Production Capacity: Fully automated, ISO & USFDA-compliant 600,000 Sq. ft. plant with zero liquid & gas discharge facility
• Delivery Time: 45-60 DAYS
• Packaging Details: Our packaging is designed to ensure maximum product safety, stability, and market appeal. We utilize high-quality raw materials (RM) and USFDA-approved packaging components, making our products ideal for export and third-party manufacturing. Key Features of Our Packaging: ✅ Attractive & Market-Differentiating Designs: Our products come with customizable branding and change parts, allowing businesses to create a distinct identity in the pharma market. ✅ Pharmaceutical-Grade Materials: We use high-density PET bottles, tamper-evident caps, and premium blister foils to maintain product integrity. ✅ Advanced Protection: Our packaging is moisture-resistant, UV-protected, and oxidation-resistant, ensuring longer shelf life and stability. ✅ High-Precision Batch Coding & Labeling: We use laser batch coding, holographic labels, and serialized QR codes for authenticity and traceability. ✅ International Standards for Export: All our packaging materials meet USFDA, EUGMP, and WHO-GMP regulations, ensuring global compliance. Our packaging solutions help PCD Pharma companies, third-party manufacturers, and exporters differentiate their products in highly competitive markets while maintaining the highest pharmaceutical standards

POVINOM is a 2% Povidone-Iodine mouth gargle used as an antiseptic solution to reduce oral and throat infections. It is effective against bacteria, viruses, fungi, and other pathogens.

• Povidone-Iodine releases free iodine, which penetrates microbial cell walls and kills bacteria, viruses, and fungi.

• Provides local antiseptic action, reducing microbial load in the oral cavity and throat.

• Sore throat and pharyngitis

• Gingivitis and oral infections

• Mouth ulcers

• Pre- and post-dental procedures for oral antisepsis

• Dilute as directed (usually 10 ml in 50 ml water, check label)

• Gargle for 30–60 seconds, 2–3 times daily

• Do not swallow the solution

• Avoid use in patients with iodine allergy

• Not recommended for prolonged use in thyroid disorders

• Keep out of reach of children

• Avoid swallowing the gargle

• Mild oral irritation or staining of teeth (temporary)

• Rarely, allergic reactions

• Effective antiseptic mouthwash for short-term oral hygiene and infection control

• Reduces microbial load in mouth and throat

• Safe for daily use if used as directed

Additional Information:

• Production Capacity: Fully automated, ISO & USFDA-compliant 600,000 Sq. ft. plant with zero liquid & gas discharge facility
• Delivery Time: 45-60 DAYS
• Packaging Details: Our packaging is designed to ensure maximum product safety, stability, and market appeal. We utilize high-quality raw materials (RM) and USFDA-approved packaging components, making our products ideal for export and third-party manufacturing. Key Features of Our Packaging: ✅ Attractive & Market-Differentiating Designs: Our products come with customizable branding and change parts, allowing businesses to create a distinct identity in the pharma market. ✅ Pharmaceutical-Grade Materials: We use high-density PET bottles, tamper-evident caps, and premium blister foils to maintain product integrity. ✅ Advanced Protection: Our packaging is moisture-resistant, UV-protected, and oxidation-resistant, ensuring longer shelf life and stability. ✅ High-Precision Batch Coding & Labeling: We use laser batch coding, holographic labels, and serialized QR codes for authenticity and traceability. ✅ International Standards for Export: All our packaging materials meet USFDA, EUGMP, and WHO-GMP regulations, ensuring global compliance. Our packaging solutions help PCD Pharma companies, third-party manufacturers, and exporters differentiate their products in highly competitive markets while maintaining the highest pharmaceutical standards.

KETLIMAC Shampoo is a scientifically formulated medicated anti-dandruff shampoo designed to provide effective relief from dandruff, seborrheic dermatitis, and fungal scalp infections. The powerful combination of Ketoconazole and Zinc Pyrithione works synergistically to eliminate dandruff-causing fungi while controlling excessive scalp flaking and itching.

Manufactured in a WHO-GMP, USFDA, and EU-GMP certified facility, KETLIMAC Shampoo ensures high purity, optimal stability, and excellent patient compliance, making it an ideal choice for PCD Pharma Franchise, third-party manufacturing, and export markets.

• Broad-spectrum imidazole antifungal
• Inhibits ergosterol synthesis in fungal cell membranes
• Effectively targets Malassezia species
• Reduces fungal load and scalp inflammation

• Controls dandruff-causing microorganisms
• Reduces flaking, itching, and scaling
• Helps normalize scalp cell turnover

Dual-Action Benefit:
✔ Eliminates dandruff at the root
✔ Soothes itchy, flaky scalp
✔ Prevents recurrence

✅ Powerful antifungal & anti-dandruff combination
✅ Clinically effective in seborrheic dermatitis
✅ Rapid relief from itching, flaking & irritation
✅ Controls excess scalp oil & microbial growth
✅ Dermatologically trusted formulation
✅ Manufactured in WHO-GMP & USFDA-certified facilities
✅ Ideal for PCD Pharma & Third-Party Manufacturing
✅ Export-quality product with EU-GMP compliance
✅ Secure bottle packaging for stability & shelf life

🔹 Dandruff & recurrent scalp flaking
🔹 Seborrheic dermatitis
🔹 Fungal scalp infections
🔹 Itchy, oily, and scaly scalp conditions
🔹 Prescribed by dermatologists
🔹 Suitable for wholesalers, stockists & international buyers

• Mild scalp irritation or dryness
• Temporary itching or hair dryness
• Rare allergic reactions

⚠️ For external use only. Avoid contact with eyes. Use under medical supervision.

✅ DMF-Grade APIs & Premium Excipients
✅ WHO-GMP Validated Manufacturing Standards
✅ Strict Microbial & Quality Control Systems
✅ Cross-Contamination-Free Production Environment
✅ High-Quality Packaging ensuring longer shelf life

✔️ PCD Pharma Franchise in Dermatology & Hair Care Segment
✔️ Third-Party Manufacturing of Ketoconazole + ZPTO Shampoo
✔️ Reliable Anti-Dandruff Shampoo Supplier in India
✔️ WHO-GMP Certified Dermatology Product Manufacturer
✔️ USFDA & EU-GMP Approved Hair & Scalp Care Products for Export

Additional Information:

• Production Capacity: Fully automated, ISO & USFDA-compliant 600,000 Sq. ft. plant with zero liquid & gas discharge facility
• Delivery Time: 45-60 DAYS
• Packaging Details: Our packaging is designed to ensure maximum product safety, stability, and market appeal. We utilize high-quality raw materials (RM) and USFDA-approved packaging components, making our products ideal for export and third-party manufacturing. Key Features of Our Packaging: ✅ Attractive & Market-Differentiating Designs: Our products come with customizable branding and change parts, allowing businesses to create a distinct identity in the pharma market. ✅ Pharmaceutical-Grade Materials: We use high-density PET bottles, tamper-evident caps, and premium blister foils to maintain product integrity. ✅ Advanced Protection: Our packaging is moisture-resistant, UV-protected, and oxidation-resistant, ensuring longer shelf life and stability. ✅ High-Precision Batch Coding & Labeling: We use laser batch coding, holographic labels, and serialized QR codes for authenticity and traceability. ✅ International Standards for Export: All our packaging materials meet USFDA, EUGMP, and WHO-GMP regulations, ensuring global compliance. Our packaging solutions help PCD Pharma companies, third-party manufacturers, and exporters differentiate their products in highly competitive markets while maintaining the highest pharmaceutical standards.

DECAPRIDE-50 MG Injection is a potent corticosteroid formulation designed for rapid control of severe inflammation, allergic reactions, and immune-mediated conditions. It delivers fast therapeutic action in emergency and critical care settings where immediate anti-inflammatory and immunosuppressive effects are required.

With its proven efficacy and rapid onset of action, DECAPRIDE-50 MG Injection is widely used in hospitals, specialty clinics, and emergency care units.

Manufactured in a WHO-GMP compliant, quality-controlled facility, DECAPRIDE-50 MG Injection ensures sterility, purity, and consistent potency — making it ideal for institutional supply, PCD Pharma Franchise, third-party manufacturing, and export markets.

Deflazacort / Corticosteroid Equivalent (50 mg):
A powerful anti-inflammatory and immunosuppressive agent that works by:

• Inhibiting inflammatory mediators
• Reducing immune system overactivity
• Controlling allergic and autoimmune responses
• Minimizing tissue swelling and redness

Its rapid pharmacological action makes it effective in managing acute inflammatory and hypersensitivity conditions.

✅ Rapid Relief in Acute Inflammatory Conditions
✅ Effective in Severe Allergic Reactions
✅ Strong Immunosuppressive Action
✅ Suitable for Hospital & Clinical Use
✅ Sterile & Safe Injectable Formulation
✅ WHO-GMP Certified Manufacturing Facility
✅ Ideal for Institutional & Government Supply
✅ Export-Quality Standards
✅ Secure, Tamper-Proof Packaging

🏥 Hospitals & Emergency Care Units
🌡 Severe allergic reactions & anaphylactic conditions
🫁 Acute asthma exacerbations
🦴 Autoimmune & inflammatory disorders
🧠 Neurological inflammatory conditions (as prescribed)
📦 Suitable for stockists, institutional suppliers & international importers

• Temporary rise in blood sugar
• Fluid retention
• Increased appetite
• Gastric irritation
• Mood changes (rare)

⚠️ To be administered strictly under medical supervision. Use cautiously in patients with diabetes, hypertension, infections, or gastrointestinal disorders.

✅ Premium Quality Active Ingredient: Sourced from certified manufacturers with strict quality validation.
✅ Sterile Injectable Manufacturing: Produced in controlled aseptic environments.
✅ Stringent Microbial Testing: Ensures safety and compliance with pharmacopeial standards.
✅ Cross-Contamination Control: Dedicated injectable production zones.
✅ Stable & Secure Packaging: Ensures product integrity during transport and storage.
✅ Technical & Regulatory Support: Comprehensive documentation support for domestic & export markets.

✔️ PCD Pharma Franchise for Injectable Corticosteroids
✔️ Third-Party Manufacturing of Sterile Injections
✔️ WHO-GMP Certified Injectable Manufacturer
✔️ Hospital Supply of Anti-Inflammatory Injections
✔️ Export-Quality Sterile Corticosteroid Injection
✔️ Institutional & Government Tender Supply Products

Additional Information:

• Production Capacity: Fully automated, ISO & USFDA-compliant 600,000 Sq. ft. plant with zero liquid & gas discharge facility
• Delivery Time: 45-60 days
• Packaging Details: Our packaging is designed to ensure maximum product safety, stability, and market appeal. We utilize high-quality raw materials (RM) and USFDA-approved packaging components, making our products ideal for export and third-party manufacturing. Key Features of Our Packaging: ✅ Attractive & Market-Differentiating Designs: Our products come with customizable branding and change parts, allowing businesses to create a distinct identity in the pharma market. ✅ Pharmaceutical-Grade Materials: We use high-density PET bottles, tamper-evident caps, and premium blister foils to maintain product integrity. ✅ Advanced Protection: Our packaging is moisture-resistant, UV-protected, and oxidation-resistant, ensuring longer shelf life and stability. ✅ High-Precision Batch Coding & Labeling: We use laser batch coding, holographic labels, and serialized QR codes for authenticity and traceability. ✅ International Standards for Export: All our packaging materials meet USFDA, EUGMP, and WHO-GMP regulations, ensuring global compliance. Our packaging solutions help PCD Pharma companies, third-party manufacturers, and exporters differentiate their products in highly competitive markets while maintaining the highest pharmaceutical standards.

AFTERSPAS-P is a clinically trusted antispasmodic and pain-relief formulation designed to provide fast and effective relief from abdominal cramps, spasmodic pain, and gastrointestinal discomfort. It is commonly prescribed for conditions such as stomach cramps, intestinal colic, menstrual pain, and spasms associated with gastrointestinal disorders.

With its powerful dual-action mechanism, AFTERSPAS-P relaxes smooth muscles and relieves pain, helping patients experience quick comfort and improved daily functioning.

Manufactured in a WHO-GMP, USFDA, and EUGMP-certified facility, AFTERSPAS-P ensures high purity, consistent quality, excellent stability, and superior patient compliance—making it ideal for PCD Pharma Franchise, third-party manufacturing, and export markets.

Antispasmodic Component (e.g., Drotaverine Hydrochloride):
Relaxes smooth muscles of the gastrointestinal and genitourinary tract, effectively reducing spasms and cramping pain.

Analgesic Component (e.g., Paracetamol):
Provides pain relief and reduces associated discomfort or mild inflammation.

This balanced combination ensures quick relief from spasmodic pain while addressing underlying muscle contractions.

✅ Fast relief from abdominal cramps & spasms
✅ Effective in gastrointestinal & menstrual pain
✅ Relaxes smooth muscles without affecting normal motility
✅ Dual-action formula for enhanced pain control
✅ Improves patient comfort & daily activity
✅ Suitable for short-term symptomatic management
✅ Manufactured in WHO-GMP & USFDA-certified facilities
✅ EUGMP-compliant for regulated export markets
✅ PCD Pharma Franchise & third-party manufacturing ready
✅ Premium blister packaging for enhanced stability & shelf life

✔️ Abdominal colic
✔️ Gastrointestinal spasms
✔️ Irritable bowel-related cramps
✔️ Menstrual cramps (dysmenorrhea)
✔️ Post-operative or procedure-related spasmodic pain

Dose: As prescribed by the physician

Usually taken after meals

Follow healthcare professional’s advice for safe and effective use

Mild nausea

Dizziness

Dry mouth

Allergic reactions (rare)

(Use under medical supervision.)

✅ DMF-grade raw materials ensuring superior safety
✅ Clinically established antispasmodic & analgesic combination
✅ Strict quality control & contamination prevention
✅ High stability formulation for extended shelf life
✅ Ideal for domestic and international markets

✔️ PCD Pharma Franchise for antispasmodic & pain relief tablets
✔️ Third-party manufacturing of Drotaverine + Paracetamol tablets
✔️ WHO-GMP certified gastrointestinal medicine manufacturer
✔️ USFDA & EUGMP approved pharmaceutical products for export

Additional Information:

• Production Capacity: Fully automated, ISO & USFDA-compliant 600,000 Sq. ft. plant with zero liquid & gas discharge facility
• Delivery Time: 45-60 DAYS
• Packaging Details: Our packaging is designed to ensure maximum product safety, stability, and market appeal. We utilize high-quality raw materials (RM) and USFDA-approved packaging components, making our products ideal for export and third-party manufacturing. Key Features of Our Packaging: ✅ Attractive & Market-Differentiating Designs: Our products come with customizable branding and change parts, allowing businesses to create a distinct identity in the pharma market. ✅ Pharmaceutical-Grade Materials: We use high-density PET bottles, tamper-evident caps, and premium blister foils to maintain product integrity. ✅ Advanced Protection: Our packaging is moisture-resistant, UV-protected, and oxidation-resistant, ensuring longer shelf life and stability. ✅ High-Precision Batch Coding & Labeling: We use laser batch coding, holographic labels, and serialized QR codes for authenticity and traceability. ✅ International Standards for Export: All our packaging materials meet USFDA, EUGMP, and WHO-GMP regulations, ensuring global compliance. Our packaging solutions help PCD Pharma companies, third-party manufacturers, and exporters differentiate their products in highly competitive markets while maintaining the highest pharmaceutical standards.

Ofloxacin 100 mg Suspension is a widely prescribed fluoroquinolone antibiotic formulated to provide effective treatment against a broad range of bacterial infections. Specially designed in an easy-to-administer liquid form.

Manufactured in WHO-GMP compliant, quality-certified facilities, Ofloxacin 100 mg Suspension guarantees high purity, consistent potency, and optimal bioavailability.

Generic Name: Ofloxacin
Strength: 100 mg per 5 ml (or as specified)
Dosage Form: Oral Suspension
Therapeutic Class: Fluoroquinolone Antibiotic
Packaging: HDPE bottle with measuring cup / dropper (customizable)

Ofloxacin is a second-generation fluoroquinolone antibiotic known for its broad-spectrum antibacterial activity against Gram-positive and Gram-negative organisms. The suspension form is particularly beneficial in pediatric practice, where flexible dosing and ease of administration are critical.

✅ Broad-spectrum antibacterial coverage
✅ Effective against Gram-positive & Gram-negative pathogens
✅ Rapid onset of action
✅ High oral bioavailability
✅ Pediatric-friendly suspension form
✅ Accurate dosing with measuring device
✅ Pleasant taste for better compliance
✅ Reliable therapeutic outcomes
✅ Manufactured under strict GMP standards

Weight-based dosing ensures safety and effectiveness in children.

Ideal for patients who cannot swallow tablets or capsules.

Allows physicians to tailor therapy according to severity and age.

Palatable flavor improves adherence to the full antibiotic course.

Dose: As directed by the physician.

✅ Premium-grade API sourcing
✅ Excellent palatability for pediatric compliance
✅ Reliable therapeutic outcomes
✅ Stringent quality assurance
✅ Competitive pricing structure
✅ Strong supply chain management
✅ Attractive franchise margins
✅ Custom manufacturing solutions

✔️ Monopoly rights (district/state level)
✔️ Attractive promotional inputs
✔️ Competitive pricing & high margins
✔️ Marketing support materials
✔️ Timely product delivery
✔️ Long shelf life for better inventory management

We offer third-party manufacturing solutions for Ofloxacin 100 mg Suspension with:

✔️ Pediatricians
✔️ General Physicians
✔️ ENT Specialists
✔️ Family Practitioners
✔️ Rural healthcare providers
✔️ Hospital supply chains
✔️ PCD Pharma Franchise distributors
✔️ Export pharmaceutical traders

Additional Information:

• Production Capacity: Fully automated, ISO & USFDA-compliant 600,000 Sq. ft. plant with zero liquid & gas discharge facility
• Delivery Time: 45-60 DAYS
• Packaging Details: Our packaging is designed to ensure maximum product safety, stability, and market appeal. We utilize high-quality raw materials (RM) and USFDA-approved packaging components, making our products ideal for export and third-party manufacturing. Key Features of Our Packaging: ✅ Attractive & Market-Differentiating Designs: Our products come with customizable branding and change parts, allowing businesses to create a distinct identity in the pharma market. ✅ Pharmaceutical-Grade Materials: We use high-density PET bottles, tamper-evident caps, and premium blister foils to maintain product integrity. ✅ Advanced Protection: Our packaging is moisture-resistant, UV-protected, and oxidation-resistant, ensuring longer shelf life and stability. ✅ High-Precision Batch Coding & Labeling: We use laser batch coding, holographic labels, and serialized QR codes for authenticity and traceability. ✅ International Standards for Export: All our packaging materials meet USFDA, EUGMP, and WHO-GMP regulations, ensuring global compliance. Our packaging solutions help PCD Pharma companies, third-party manufacturers, and exporters differentiate their products in highly competitive markets while maintaining the highest pharmaceutical standards.

KEONA is a medicated antifungal cleansing bar formulated with Ketoconazole 1.0% w/w Soap, designed for effective management of superficial fungal infections and maintenance of healthy skin hygiene. It delivers targeted antifungal therapy along with daily cleansing, helping reduce infection spread and recurrence.

Manufactured in a WHO-GMP compliant facility using high-quality APIs and dermatologically compatible excipients, KEONA ensures uniform drug dispersion, consistent therapeutic efficacy, and enhanced patient compliance — making it suitable for PCD Pharma Franchise, third-party manufacturing, and export markets.

Ketoconazole (1.0% w/w):
A broad-spectrum imidazole antifungal agent that inhibits ergosterol synthesis, an essential component of fungal cell membranes. By disrupting membrane integrity, it increases cellular permeability, leading to fungal cell death.

Ketoconazole is effective against dermatophytes, yeasts, and other pathogenic fungi responsible for common skin infections. Regular cleansing with KEONA helps reduce fungal load, relieve itching, and support faster recovery.

The medicated soap base ensures even distribution of the active ingredient while maintaining proper skin hygiene.

✅ Broad-Spectrum Antifungal Action
✅ Effective for Ringworm, Athlete’s Foot & Jock Itch
✅ Helps Reduce Itching, Redness & Scaling
✅ Supports Prevention of Recurrent Fungal Infections
✅ Medicated Cleansing with Uniform Drug Distribution
✅ Dermatologically Designed Formulation
✅ WHO-GMP Manufactured
✅ Suitable for PCD Pharma & Third-Party Manufacturing
✅ Export-Quality Standards

✔️ Patients with superficial fungal skin infections
✔️ Individuals prone to recurrent fungal conditions
✔️ Excess sweating leading to fungal growth
✔️ Infections in skin folds and moist areas
✔️ Dermatology clinics & healthcare providers
✔️ Pharmacies, distributors, stockists & international buyers

Additional Information:

• Production Capacity: Fully automated, ISO & USFDA-compliant 600,000 Sq. ft. plant with zero liquid & gas discharge facility
• Delivery Time: 45-60 days
• Packaging Details: Our packaging is designed to ensure maximum product safety, stability, and market appeal. We utilize high-quality raw materials (RM) and USFDA-approved packaging components, making our products ideal for export and third-party manufacturing. Key Features of Our Packaging: ✅ Attractive & Market-Differentiating Designs: Our products come with customizable branding and change parts, allowing businesses to create a distinct identity in the pharma market. ✅ Pharmaceutical-Grade Materials: We use high-density PET bottles, tamper-evident caps, and premium blister foils to maintain product integrity. ✅ Advanced Protection: Our packaging is moisture-resistant, UV-protected, and oxidation-resistant, ensuring longer shelf life and stability. ✅ High-Precision Batch Coding & Labeling: We use laser batch coding, holographic labels, and serialized QR codes for authenticity and traceability. ✅ International Standards for Export: All our packaging materials meet USFDA, EUGMP, and WHO-GMP regulations, ensuring global compliance. Our packaging solutions help PCD Pharma companies, third-party manufacturers, and exporters differentiate their products in highly competitive markets while maintaining the highest pharmaceutical standards.

AUTOBACT-KID is a scientifically formulated pediatric antibiotic tablet that combines Amoxicillin 200 mg with Clavulanic Acid 28.5 mg in a convenient oral dosage form. This dual-action combination provides broad-spectrum antibacterial coverage, including activity against beta-lactamase–producing resistant strains, making it highly effective in treating common pediatric infections.

Manufactured in a WHO-GMP compliant facility with stringent quality control, AUTOBACT-KID Tablets ensure purity, potency, and batch-to-batch consistency. The product is ideal for PCD Pharma Franchise, third-party manufacturing, hospital supply, and regulated export markets.

Each tablet contains:

• Amoxicillin Trihydrate equivalent to Amoxicillin 200 mg

• Clavulanic Acid equivalent to 28.5 mg

• Excipients q.s. for tablet formulation

Dosage form: Film-coated pediatric tablet
Packaging: High-quality blister pack for protection and stability

Amoxicillin is a broad-spectrum beta-lactam antibiotic that inhibits bacterial cell wall synthesis by binding to penicillin-binding proteins, resulting in bactericidal activity. It effectively targets susceptible Gram-positive and Gram-negative bacteria.

Clavulanic Acid inhibits beta-lactamase enzymes produced by resistant bacteria, preventing inactivation of Amoxicillin and restoring its antibacterial effectiveness.

• Bactericidal effect from Amoxicillin

• Protection against beta-lactamase–producing bacteria

• Broader spectrum of action

• Higher clinical success rates

AUTOBACT-KID Tablets are indicated for infections caused by susceptible organisms, including:

• Respiratory tract infections: Tonsillitis, pharyngitis, sinusitis, bronchitis

• Ear infections: Acute otitis media

• Urinary tract infections: Pediatric cystitis

• Skin and soft tissue infections: Impetigo, cellulitis, wound infections

• Dental infections: Dental abscess, gingivitis

Dosage: As directed by the physician based on age, body weight, and infection severity.

Administration: Swallow whole with water. Tablets are formulated for pediatric use, ensuring accurate dosing and compliance. Complete the full course as prescribed to prevent resistance.

Each batch undergoes assay, content uniformity, microbial limits, and stability testing to ensure consistent therapeutic performance.Packaging

Additional Information:

• Production Capacity: Fully automated, ISO & USFDA-compliant 600,000 Sq. ft. plant with zero liquid & gas discharge facility
• Delivery Time: 45-60 DAYS
• Packaging Details: Our packaging is designed to ensure maximum product safety, stability, and market appeal. We utilize high-quality raw materials (RM) and USFDA-approved packaging components, making our products ideal for export and third-party manufacturing. Key Features of Our Packaging: ✅ Attractive & Market-Differentiating Designs: Our products come with customizable branding and change parts, allowing businesses to create a distinct identity in the pharma market. ✅ Pharmaceutical-Grade Materials: We use high-density PET bottles, tamper-evident caps, and premium blister foils to maintain product integrity. ✅ Advanced Protection: Our packaging is moisture-resistant, UV-protected, and oxidation-resistant, ensuring longer shelf life and stability. ✅ High-Precision Batch Coding & Labeling: We use laser batch coding, holographic labels, and serialized QR codes for authenticity and traceability. ✅ International Standards for Export: All our packaging materials meet USFDA, EUGMP, and WHO-GMP regulations, ensuring global compliance. Our packaging solutions help PCD Pharma companies, third-party manufacturers, and exporters differentiate their products in highly competitive markets while maintaining the highest pharmaceutical standards.

Brand Name: NASOWIPE
Dosage Form: Nasal drops
Strength: Xylometazoline 0.1% w/v + Benzalkonium Chloride 0.02% w/v
Class: Nasal decongestant

• Xylometazoline 1 mg – nasal decongestant

• Benzalkonium Chloride 0.2 mg – preservative

• Sterile water q.s.

• Xylometazoline: Alpha-adrenergic agonist → vasoconstriction → reduces nasal congestion

• Benzalkonium Chloride: Preservative; mild antiseptic

• Nasal congestion: common cold, allergic rhinitis, sinusitis

• Pre-nasal examination or minor procedures

• Adults & children >12 yrs: 2–3 drops/nostril, 2–3 times daily

• Children 6–12 yrs: 1–2 drops/nostril, 2 times daily

• Max duration: 3–5 days

Instructions: Wash hands, avoid touching dropper, blow nose gently after 5–10 min

• Hypersensitivity to Xylometazoline or Benzalkonium Chloride

• Severe hypertension, heart disease, glaucoma

• MAO inhibitor use

• Short-term use only (≤5 days) to prevent rebound congestion

• Avoid in children <6 yrs without doctor guidance

• Caution in cardiovascular disorders

• Mild stinging, burning, dryness

• Rare: sneezing, headache, rebound congestion, palpitations

• Store below 25°C, protect from light

• Keep bottle closed; discard 4 weeks after opening

NASOWIPE is a fast-acting nasal decongestant providing rapid relief from nasal blockage in colds, allergies, and sinusitis. Short-term use ensures effective decongestion with minimal side effects.

Additional Information:

• Production Capacity: Fully automated, ISO & USFDA-compliant 600,000 Sq. ft. plant with zero liquid & gas discharge facility
• Delivery Time: 45-60 DAYS
• Packaging Details: Our packaging is designed to ensure maximum product safety, stability, and market appeal. We utilize high-quality raw materials (RM) and USFDA-approved packaging components, making our products ideal for export and third-party manufacturing. Key Features of Our Packaging: ✅ Attractive & Market-Differentiating Designs: Our products come with customizable branding and change parts, allowing businesses to create a distinct identity in the pharma market. ✅ Pharmaceutical-Grade Materials: We use high-density PET bottles, tamper-evident caps, and premium blister foils to maintain product integrity. ✅ Advanced Protection: Our packaging is moisture-resistant, UV-protected, and oxidation-resistant, ensuring longer shelf life and stability. ✅ High-Precision Batch Coding & Labeling: We use laser batch coding, holographic labels, and serialized QR codes for authenticity and traceability. ✅ International Standards for Export: All our packaging materials meet USFDA, EUGMP, and WHO-GMP regulations, ensuring global compliance. Our packaging solutions help PCD Pharma companies, third-party manufacturers, and exporters differentiate their products in highly competitive markets while maintaining the highest pharmaceutical standards.

Paracetamol 250 mg + Mefenamic Acid 100 mg is a clinically trusted combination used for the management of fever, mild to moderate pain, and inflammatory conditions. This dual-action formulation provides rapid symptomatic relief by combining the antipyretic effect of Paracetamol with the anti-inflammatory and analgesic properties of Mefenamic Acid.

Manufactured in WHO-GMP compliant facilities with stringent quality control standards, this formulation ensures purity, consistent potency, optimal bioavailability, and reliable therapeutic performance. It is well-suited for domestic markets, PCD Pharma Franchise, third-party manufacturing, and export opportunities.

• Acts as an antipyretic (reduces fever)

• Provides central analgesic action

• Blocks pain signals in the brain

• Offers quick relief from headache, body ache, and fever

• Non-steroidal anti-inflammatory drug (NSAID)

• Inhibits prostaglandin synthesis

• Reduces inflammation, swelling, and pain

• Effective in spasmodic and inflammatory pain conditions

Together, they provide enhanced pain relief and faster reduction of fever.

✅ Dual-action formula for fever & pain
✅ Rapid onset of action
✅ Effective in inflammatory conditions
✅ Provides stronger relief than single-drug therapy
✅ Suitable for pediatric use (as per physician advice)
✅ Reliable safety profile when used as directed
✅ Manufactured under strict GMP standards
✅ Ideal for PCD & third-party manufacturing

✔️ Fever (viral or bacterial origin)
✔️ Headache
✔️ Toothache
✔️ Ear pain
✔️ Body ache
✔️ Musculoskeletal pain
✔️ Post-vaccination fever
✔️ Dysmenorrhea (menstrual pain)
✔️ Inflammatory pain conditions

Dose: As directed by the physician

• Usually administered 2–3 times daily depending on severity

• Preferably taken after food to reduce gastric irritation

• Do not exceed recommended dosage

• Shake well before use (if suspension form)

Generally well tolerated when used under medical supervision.

• Nausea

• Gastric discomfort

• Mild acidity

• Dizziness (rare)

• Use cautiously in patients with gastric ulcers

• Avoid overdose to prevent liver toxicity (due to Paracetamol)

• Not recommended without medical advice in severe liver or kidney disease

✅ Clinically proven and widely prescribed combination
✅ Effective fever reduction with added anti-inflammatory action
✅ Premium-quality API sourcing
✅ Stable formulation with consistent results
✅ Strong demand in pediatric and general practice
✅ Attractive commercial margins
✅ Suitable for franchise and export markets

✔️ PCD Pharma Franchise for pediatric and general range
✔️ Third-party manufacturing of Paracetamol combinations
✔️ WHO-GMP certified manufacturer
✔️ Export-ready analgesic and antipyretic formulations

Additional Information:

• Production Capacity: Fully automated, ISO & USFDA-compliant 600,000 Sq. ft. plant with zero liquid & gas discharge facility
• Delivery Time: 45-60 DAYS
• Packaging Details: Our packaging is designed to ensure maximum product safety, stability, and market appeal. We utilize high-quality raw materials (RM) and USFDA-approved packaging components, making our products ideal for export and third-party manufacturing. Key Features of Our Packaging: ✅ Attractive & Market-Differentiating Designs: Our products come with customizable branding and change parts, allowing businesses to create a distinct identity in the pharma market. ✅ Pharmaceutical-Grade Materials: We use high-density PET bottles, tamper-evident caps, and premium blister foils to maintain product integrity. ✅ Advanced Protection: Our packaging is moisture-resistant, UV-protected, and oxidation-resistant, ensuring longer shelf life and stability. ✅ High-Precision Batch Coding & Labeling: We use laser batch coding, holographic labels, and serialized QR codes for authenticity and traceability. ✅ International Standards for Export: All our packaging materials meet USFDA, EUGMP, and WHO-GMP regulations, ensuring global compliance. Our packaging solutions help PCD Pharma companies, third-party manufacturers, and exporters differentiate their products in highly competitive markets while maintaining the highest pharmaceutical standards.

KEONA Soap contains Ketoconazole 1.0% w/w, a proven imidazole antifungal agent that helps eliminate fungal pathogens while gently cleansing the skin. It is specially formulated to manage fungal skin infections, dandruff-related body lesions, and recurrent itching, making it suitable for daily hygiene in affected individuals.

Manufactured in a WHO-GMP, USFDA, and EU-GMP certified facility, KEONA Soap ensures consistent quality, optimal stability, and excellent patient acceptability, making it an ideal product for PCD Pharma Franchise, third-party manufacturing, and export markets.

• Broad-spectrum imidazole antifungal
• Inhibits ergosterol synthesis in fungal cell membranes
• Controls growth of dermatophytes and yeasts
• Reduces itching, scaling, and redness

Regular use helps maintain fungal control while cleansing, reducing recurrence of infection.

✅ Medicated antifungal cleansing soap
✅ Helps control fungal skin infections & itching
✅ Effective against dermatophytes & yeast infections
✅ Gentle on skin with daily-use compatibility
✅ Helps prevent recurrence when used regularly
✅ Manufactured in WHO-GMP & USFDA-certified facilities
✅ Suitable for PCD Pharma & Third-Party Manufacturing
✅ Export-quality product with EU-GMP compliance
✅ Hygienic packaging for longer shelf life

�� Tinea corporis (Ringworm)
�� Tinea cruris (Jock itch)
�� Tinea pedis (Athlete’s foot – adjunct hygiene)
�� Fungal skin infections with itching & scaling
�� Seborrheic dermatitis-related body lesions
�� Suitable for dermatology prescriptions
�� Ideal for wholesalers, stockists & international buyers

• Mild skin dryness
• Temporary irritation in sensitive skin
• Rare allergic reactions

⚠️ For external use only. Avoid contact with eyes. Discontinue use if severe irritation occurs.

✅ Premium Quality API & Base Ingredients
✅ WHO-GMP Validated Manufacturing Standards
✅ Strict Quality & Microbial Control Systems
✅ Cross-Contamination-Free Production Environment
✅ High-Quality Packaging ensuring product stability

✔️ PCD Pharma Franchise in Dermatology Segment
✔️ Third-Party Manufacturing of Ketoconazole Soap
✔️ Reliable Antifungal Bathing Soap Supplier in India
✔️ WHO-GMP Certified Dermatology Product Manufacturer
✔️ USFDA & EU-GMP Approved Antifungal Products for Export

Additional Information:

• Production Capacity: Fully automated, ISO & USFDA-compliant 600,000 Sq. ft. plant with zero liquid & gas discharge facility
• Delivery Time: 45-60 DAYS
• Packaging Details: Our packaging is designed to ensure maximum product safety, stability, and market appeal. We utilize high-quality raw materials (RM) and USFDA-approved packaging components, making our products ideal for export and third-party manufacturing. Key Features of Our Packaging: ✅ Attractive & Market-Differentiating Designs: Our products come with customizable branding and change parts, allowing businesses to create a distinct identity in the pharma market. ✅ Pharmaceutical-Grade Materials: We use high-density PET bottles, tamper-evident caps, and premium blister foils to maintain product integrity. ✅ Advanced Protection: Our packaging is moisture-resistant, UV-protected, and oxidation-resistant, ensuring longer shelf life and stability. ✅ High-Precision Batch Coding & Labeling: We use laser batch coding, holographic labels, and serialized QR codes for authenticity and traceability. ✅ International Standards for Export: All our packaging materials meet USFDA, EUGMP, and WHO-GMP regulations, ensuring global compliance. Our packaging solutions help PCD Pharma companies, third-party manufacturers, and exporters differentiate their products in highly competitive markets while maintaining the highest pharmaceutical standards.

Brand Name: HEXICO
Dosage Form: Mouthwash
Strength: Chlorhexidine Gluconate 0.2% w/v + Sodium Benzoate 0.02% w/v
Class: Antimicrobial / Oral antiseptic

• Chlorhexidine Gluconate 0.2% – active antiseptic

• Sodium Benzoate 0.02% – preservative

• Purified water q.s.

• Chlorhexidine: Disrupts bacterial cell membranes → bactericidal

• Sodium Benzoate: Preservative; maintains sterility

• Gingivitis, periodontitis

• Plaque control

• Post-dental surgery oral hygiene

• Oral infections prevention

• Adults & children >12 yrs: 10–15 mL, rinse 30–60 sec, twice daily

• Children <12 yrs: Half adult dose

• Spit out; do not swallow; avoid eating/drinking 30 min after use

• Allergy to Chlorhexidine or preservatives

• Topical use only; avoid swallowing

• Short-term use to prevent mucosal irritation

• May stain teeth/tongue; avoid anionic toothpaste concurrently

• Temporary burning, altered taste

• Rare: oral irritation, allergy, staining

• Store 2–25°C, protect from light

• Keep bottle closed; discard after 6 months of opening

HEXICO is a broad-spectrum antimicrobial mouthwash that prevents plaque, gingivitis, and oral infections, supports post-surgical oral care, and ensures oral hygiene with minimal systemic absorption.

Additional Information:

• Production Capacity: Fully automated, ISO & USFDA-compliant 600,000 Sq. ft. plant with zero liquid & gas discharge facility
• Delivery Time: 45-60 DAYS
• Packaging Details: Our packaging is designed to ensure maximum product safety, stability, and market appeal. We utilize high-quality raw materials (RM) and USFDA-approved packaging components, making our products ideal for export and third-party manufacturing. Key Features of Our Packaging: ✅ Attractive & Market-Differentiating Designs: Our products come with customizable branding and change parts, allowing businesses to create a distinct identity in the pharma market. ✅ Pharmaceutical-Grade Materials: We use high-density PET bottles, tamper-evident caps, and premium blister foils to maintain product integrity. ✅ Advanced Protection: Our packaging is moisture-resistant, UV-protected, and oxidation-resistant, ensuring longer shelf life and stability. ✅ High-Precision Batch Coding & Labeling: We use laser batch coding, holographic labels, and serialized QR codes for authenticity and traceability. ✅ International Standards for Export: All our packaging materials meet USFDA, EUGMP, and WHO-GMP regulations, ensuring global compliance. Our packaging solutions help PCD Pharma companies, third-party manufacturers, and exporters differentiate their products in highly competitive markets while maintaining the highest pharmaceutical standards.

GO-SPOT is a dermatologist-trusted triple-combination depigmenting formulation designed to effectively manage melasma, dark spots, chloasma, post-inflammatory hyperpigmentation, and uneven skin tone. The synergistic action of Hydroquinone, Tretinoin, and Mometasone delivers visible skin lightening while controlling inflammation and irritation.

Manufactured in a WHO-GMP, USFDA, and EU-GMP certified facility, GO-SPOT ensures high purity, formulation stability, and excellent patient compliance, making it an ideal choice for PCD Pharma Franchise, third-party manufacturing, and export markets.

• Gold-standard depigmenting agent
• Inhibits tyrosinase enzyme
• Reduces melanin synthesis
• Lightens dark patches and pigmentation

• Retinoid that increases epidermal cell turnover
• Enhances penetration of Hydroquinone
• Promotes skin renewal and texture improvement

• Mild-to-moderate potency corticosteroid
• Reduces inflammation, redness, and irritation
• Improves tolerability of depigmenting therapy

Triple-Action Advantage:
✔ Faster pigment reduction
✔ Reduced inflammation & irritation
✔ Improved skin tone uniformity

✅ Clinically proven triple-combination therapy
✅ Effective in melasma & hyperpigmentation disorders
✅ Reduces dark spots and uneven skin tone
✅ Improves skin texture & appearance
✅ Dermatologist-preferred depigmenting formula
✅ Manufactured in WHO-GMP & USFDA-certified facilities
✅ Suitable for PCD Pharma & Third-Party Manufacturing
✅ Export-quality formulation with EU-GMP compliance
✅ Tube packaging ensures stability & hygiene

🔹 Melasma & chloasma
🔹 Post-inflammatory hyperpigmentation
🔹 Dark spots & sun-induced pigmentation
🔹 Uneven skin tone
🔹 Dermatologist-prescribed depigmenting therapy
🔹 Suitable for wholesalers, stockists & international buyers

• Mild skin irritation or redness
• Temporary burning or dryness
• Rare steroid-related effects with prolonged misuse

⚠️ For external use only. Use strictly under medical supervision. Prolonged or unsupervised use should be avoided.

✅ DMF-Grade APIs & Premium Excipients
✅ WHO-GMP Validated Manufacturing Standards
✅ Strict Quality & Microbial Control Systems
✅ Cross-Contamination-Free Production Environment
✅ High-Quality Packaging for extended shelf life

✔️ PCD Pharma Franchise in Dermatology & Cosmeceuticals
✔️ Third-Party Manufacturing of Triple Combination Creams
✔️ Reliable Melasma & Pigmentation Treatment Supplier
✔️ WHO-GMP Certified Dermatology Manufacturer
✔️ USFDA & EU-GMP Approved Skin Care Products for Export

Additional Information:

• Production Capacity: Fully automated, ISO & USFDA-compliant 600,000 Sq. ft. plant with zero liquid & gas discharge facility
• Delivery Time: 45-60 DAYS
• Packaging Details: Our packaging is designed to ensure maximum product safety, stability, and market appeal. We utilize high-quality raw materials (RM) and USFDA-approved packaging components, making our products ideal for export and third-party manufacturing. Key Features of Our Packaging: ✅ Attractive & Market-Differentiating Designs: Our products come with customizable branding and change parts, allowing businesses to create a distinct identity in the pharma market. ✅ Pharmaceutical-Grade Materials: We use high-density PET bottles, tamper-evident caps, and premium blister foils to maintain product integrity. ✅ Advanced Protection: Our packaging is moisture-resistant, UV-protected, and oxidation-resistant, ensuring longer shelf life and stability. ✅ High-Precision Batch Coding & Labeling: We use laser batch coding, holographic labels, and serialized QR codes for authenticity and traceability. ✅ International Standards for Export: All our packaging materials meet USFDA, EUGMP, and WHO-GMP regulations, ensuring global compliance. Our packaging solutions help PCD Pharma companies, third-party manufacturers, and exporters differentiate their products in highly competitive markets while maintaining the highest pharmaceutical standards.

FEBUGRIP 40 is a clinically established anti-gout medication formulated with Febuxostat 40 mg, a potent and selective xanthine oxidase inhibitor. It is designed to effectively lower elevated serum uric acid levels, prevent urate crystal deposition, and reduce the frequency and severity of gout attacks.

Manufactured in a WHO-GMP, USFDA, and EUGMP–certified facility, FEBUGRIP 40 ensures high purity, consistent quality, optimal bioavailability, and excellent patient compliance. It is an ideal product for PCD Pharma Franchise, third-party manufacturing, and regulated export markets.

Febuxostat 40 mg:

• Inhibits xanthine oxidase, the enzyme responsible for uric acid production

• Significantly reduces serum uric acid concentration

• Prevents formation and deposition of urate crystals in joints

• Helps in long-term control of chronic gout and hyperuricemia

• Reduces joint pain, inflammation, and recurrence of gout flares

✅ Powerful uric acid–lowering therapy
✅ Effective in chronic gout & hyperuricemia
✅ Reduces frequency of acute gout attacks
✅ Suitable for patients intolerant to allopurinol
✅ Improves joint comfort and quality of life
✅ Once-daily dosing improves compliance
✅ WHO-GMP & USFDA-certified manufacturing
✅ EUGMP-compliant for export markets
✅ PCD Pharma & third-party manufacturing ready
✅ Alu-Alu blister packaging for maximum stability & longer shelf life

✔️ Patients suffering from chronic gout
✔️ Individuals with elevated serum uric acid levels
✔️ Patients with recurrent gout attacks
✔️ Patients not adequately controlled on other urate-lowering therapies
✔️ Long-term management of hyperuricemia-related joint disorders

• Recommended Dose: As prescribed by the physician

• Generally administered once daily, with or without food

• Dose adjustment based on serum uric acid levels

• Nausea or headache

• Dizziness or fatigue

• Mild elevation of liver enzymes

• Skin rash (rare)

(Most side effects are temporary and manageable under medical supervision)

✅ DMF-Grade API & Premium Excipients
Ensures superior safety, efficacy, and batch consistency

✅ Clinically Proven Molecule
Globally trusted for effective gout and hyperuricemia management

✅ Strict Quality & Safety Standards
Low-humidity airlock cubicles and cross-contamination prevention

✅ Superior Packaging & Storage
Alu-Alu blister ensures enhanced stability and extended shelf life

✔️ PCD Pharma Franchise for Anti-Gout Medicines
✔️ Third-Party Manufacturing of Febuxostat Tablets IP
✔️ Best Gout & Hyperuricemia Medicine Supplier in India
✔️ WHO-GMP Certified Febuxostat Manufacturer
✔️ USFDA & EUGMP Approved Gout Medicines for Export

Additional Information:

• Production Capacity: Fully automated, ISO & USFDA-compliant 600,000 Sq. ft. plant with zero liquid & gas discharge facility
• Delivery Time: 45-60 DAYS
• Packaging Details: Our packaging is designed to ensure maximum product safety, stability, and market appeal. We utilize high-quality raw materials (RM) and USFDA-approved packaging components, making our products ideal for export and third-party manufacturing. Key Features of Our Packaging: ✅ Attractive & Market-Differentiating Designs: Our products come with customizable branding and change parts, allowing businesses to create a distinct identity in the pharma market. ✅ Pharmaceutical-Grade Materials: We use high-density PET bottles, tamper-evident caps, and premium blister foils to maintain product integrity. ✅ Advanced Protection: Our packaging is moisture-resistant, UV-protected, and oxidation-resistant, ensuring longer shelf life and stability. ✅ High-Precision Batch Coding & Labeling: We use laser batch coding, holographic labels, and serialized QR codes for authenticity and traceability. ✅ International Standards for Export: All our packaging materials meet USFDA, EUGMP, and WHO-GMP regulations, ensuring global compliance. Our packaging solutions help PCD Pharma companies, third-party manufacturers, and exporters differentiate their products in highly competitive markets while maintaining the highest pharmaceutical standards.

GLUMIDE contains Glimepiride, an effective oral antidiabetic medication indicated for the management of Type 2 Diabetes Mellitus. It helps control blood glucose levels by improving insulin secretion and enhancing the body’s response to insulin, thereby supporting long-term glycemic control.

Manufactured in a WHO-GMP compliant facility, GLUMIDE meets stringent quality standards to ensure safety, efficacy, and consistency for both domestic and export markets.

Glimepiride works by:

• Stimulating pancreatic beta cells to release insulin

• Enhancing peripheral utilization of glucose

• Reducing blood glucose levels effectively

• Supporting sustained glycemic control

Its once-daily dosing regimen improves patient compliance when taken as prescribed by a healthcare professional.

✔ Effective blood glucose control in Type 2 Diabetes
✔ Supports improved insulin secretion
✔ Convenient once-daily dosing (as prescribed)
✔ Helps reduce risk of diabetes-related complications
✔ Suitable for monotherapy or combination therapy
✔ Manufactured under strict WHO-GMP quality standards
✔ Ideal for PCD Pharma Franchise & Third-Party Manufacturing

• Type 2 Diabetes Mellitus (when diet and exercise alone are insufficient)

• Can be used alone or in combination with other antidiabetic agents, as advised by a physician

To be used strictly under medical supervision.

Generally well tolerated when used appropriately. Some patients may experience:

• Hypoglycemia (low blood sugar)

• Mild gastrointestinal discomfort

• Headache

• Dizziness

Regular monitoring of blood glucose levels is recommended to ensure safe and effective therapy.

• High-quality API sourcing

• Strict in-process and finished product quality testing

• Advanced blister packaging for enhanced stability and shelf life

• Complete technical documentation support

• Suitable for domestic distribution and export markets

Dosage and duration should be determined by a qualified healthcare professional based on the patient’s clinical condition and glycemic response. Regular blood sugar monitoring and adherence to medical advice are essential for optimal diabetes management.

Additional Information:

• Production Capacity: Fully automated, ISO & USFDA-compliant 600,000 Sq. ft. plant with zero liquid & gas discharge facility
• Delivery Time: 45-60 Days
• Packaging Details: Our packaging is designed to ensure maximum product safety, stability, and market appeal. We utilize high-quality raw materials (RM) and USFDA-approved packaging components, making our products ideal for export and third-party manufacturing. Key Features of Our Packaging: ✅ Attractive & Market-Differentiating Designs: Our products come with customizable branding and change parts, allowing businesses to create a distinct identity in the pharma market. ✅ Pharmaceutical-Grade Materials: We use high-density PET bottles, tamper-evident caps, and premium blister foils to maintain product integrity. ✅ Advanced Protection: Our packaging is moisture-resistant, UV-protected, and oxidation-resistant, ensuring longer shelf life and stability. ✅ High-Precision Batch Coding & Labeling: We use laser batch coding, holographic labels, and serialized QR codes for authenticity and traceability. ✅ International Standards for Export: All our packaging materials meet USFDA, EUGMP, and WHO-GMP regulations, ensuring global compliance. Our packaging solutions help PCD Pharma companies, third-party manufacturers, and exporters differentiate their products in highly competitive markets while maintaining the highest pharmaceutical standards.

TELSICAP-40 is a high-quality antihypertensive formulation containing Telmisartan 40 mg, an Angiotensin II Receptor Blocker (ARB) indicated for the management of essential hypertension. It helps effectively control blood pressure and supports long-term cardiovascular protection.

Manufactured in a WHO-GMP compliant facility adhering to stringent quality standards, TELSICAP-40 ensures consistent efficacy, safety, and reliability for domestic and international markets.

• Selectively blocks angiotensin II (AT1) receptors

• Relaxes and widens blood vessels

• Reduces systemic blood pressure

• Decreases strain on the heart

• Provides renal and cardiovascular protection in hypertensive patients

By inhibiting the vasoconstrictive effects of angiotensin II, Telmisartan supports sustained 24-hour blood pressure control with once-daily dosing.

• Effective once-daily antihypertensive therapy

• Long-acting blood pressure control

• Supports cardiovascular risk reduction

• Well-tolerated with a favorable safety profile

• Manufactured under WHO-GMP compliant standards

• Suitable for PCD Pharma Franchise & Third-Party Manufacturing

• Essential Hypertension

• Patients requiring ARB therapy for blood pressure management

• Individuals at risk of cardiovascular complications due to uncontrolled BP

To be used strictly under medical supervision.

Generally well tolerated. Some patients may experience:

• Mild dizziness

• Fatigue

• Headache

• Occasional gastrointestinal discomfort

Patients with kidney, liver, or electrolyte disorders should consult a healthcare professional before use.

• High-quality API sourcing

• Stringent in-process and finished product quality checks

• Stable formulation with optimized excipients

• Advanced blister packaging for enhanced shelf life

• Technical documentation support available

• Ideal for domestic supply and export markets

Regular blood pressure monitoring is recommended during therapy. Dosage and duration should be determined by a qualified healthcare professional based on individual patient needs.

If required, I can also create:

✔️ SEO-optimized website content
✔️ Distributor-focused promotional version
✔️ Doctor detailing (MR visual aid) content
✔️ IndiaMART / TradeIndia listing version
✔️ Export brochure content

Additional Information:

• Production Capacity: Fully automated, ISO & USFDA-compliant 600,000 Sq. ft. plant with zero liquid & gas discharge facility
• Delivery Time: 45-60 DAYS
• Packaging Details: Our packaging is designed to ensure maximum product safety, stability, and market appeal. We utilize high-quality raw materials (RM) and USFDA-approved packaging components, making our products ideal for export and third-party manufacturing. Key Features of Our Packaging: ✅ Attractive & Market-Differentiating Designs: Our products come with customizable branding and change parts, allowing businesses to create a distinct identity in the pharma market. ✅ Pharmaceutical-Grade Materials: We use high-density PET bottles, tamper-evident caps, and premium blister foils to maintain product integrity. ✅ Advanced Protection: Our packaging is moisture-resistant, UV-protected, and oxidation-resistant, ensuring longer shelf life and stability. ✅ High-Precision Batch Coding & Labeling: We use laser batch coding, holographic labels, and serialized QR codes for authenticity and traceability. ✅ International Standards for Export: All our packaging materials meet USFDA, EUGMP, and WHO-GMP regulations, ensuring global compliance. Our packaging solutions help PCD Pharma companies, third-party manufacturers, and exporters differentiate their products in highly competitive markets while maintaining the highest pharmaceutical standards.

VENTAWAY is a clinically formulated bronchodilator tablet designed to provide effective relief from bronchial asthma, chronic obstructive pulmonary disease (COPD), and other respiratory conditions. Its dual-action mechanism helps open airways, reduce bronchospasm, and improve breathing comfort, enhancing overall respiratory health.

Manufactured in a WHO-GMP-certified facility under stringent quality control standards, VENTAWAY ensures high purity, optimal bioavailability, consistent therapeutic performance, and patient-friendly dosing. It is ideally positioned for PCD Pharma Franchise, third-party manufacturing, and regulated export markets.

• Relaxes smooth muscles in the airways

• Reduces bronchospasm and airway obstruction

• Improves airflow and oxygen delivery

• Helps reduce airway inflammation and mucus production

• Relieves wheezing, shortness of breath, and chest tightness

• Supports long-term management of chronic respiratory conditions

• Clinically proven bronchodilator and anti-asthmatic therapy

• Rapid relief from asthma attacks and bronchospasm

• Supports better lung function and oxygenation

• Suitable for chronic respiratory conditions like COPD and bronchitis

• Adult-friendly oral tablet for convenient dosing

• WHO-GMP-certified manufacturing

• High-quality API and excipients for safety and efficacy

• Stable packaging for extended shelf life

• Ideal for domestic and export markets

• PCD Pharma Franchise & third-party manufacturing ready

• Bronchial asthma

• Chronic obstructive pulmonary disease (COPD)

• Bronchitis and wheezing disorders

• Allergic respiratory conditions

• Shortness of breath and bronchospasm management

• Dose: As directed by the physician

• Adult dosing based on severity of symptoms and physician recommendation

• Swallow whole with water

• Follow prescribed duration for optimal results

• Not to be used in combination with other bronchodilators without medical supervision

• Mild tremors or palpitations

• Headache or dizziness

• Gastrointestinal discomfort (nausea, upset stomach)

• Rare hypersensitivity reactions

• Clinically effective bronchodilator for acute and chronic respiratory care

• High-quality API and premium excipients for safety and efficacy

• Strict quality assurance and manufacturing compliance

• Convenient adult-friendly tablet for reliable symptom control

• Strong franchise and export potential

Ideal for partners seeking:

• Bronchodilator and anti-asthmatic tablet PCD Franchise

• Third-party manufacturing of respiratory care formulations

• WHO-GMP-certified manufacturer for adult respiratory medicines

• Export-ready asthma and COPD treatment products

Additional Information:

• Production Capacity: Fully automated, ISO & USFDA-compliant 600,000 Sq. ft. plant with zero liquid & gas discharge facility
• Delivery Time: 45-60 days
• Packaging Details: Our packaging is designed to ensure maximum product safety, stability, and market appeal. We utilize high-quality raw materials (RM) and USFDA-approved packaging components, making our products ideal for export and third-party manufacturing. Key Features of Our Packaging: ✅ Attractive & Market-Differentiating Designs: Our products come with customizable branding and change parts, allowing businesses to create a distinct identity in the pharma market. ✅ Pharmaceutical-Grade Materials: We use high-density PET bottles, tamper-evident caps, and premium blister foils to maintain product integrity. ✅ Advanced Protection: Our packaging is moisture-resistant, UV-protected, and oxidation-resistant, ensuring longer shelf life and stability. ✅ High-Precision Batch Coding & Labeling: We use laser batch coding, holographic labels, and serialized QR codes for authenticity and traceability. ✅ International Standards for Export: All our packaging materials meet USFDA, EUGMP, and WHO-GMP regulations, ensuring global compliance. Our packaging solutions help PCD Pharma companies, third-party manufacturers, and exporters differentiate their products in highly competitive markets while maintaining the highest pharmaceutical standards.

AFTERGEST is a clinically trusted hormonal therapy formulated with Dydrogesterone 10 mg, a selective synthetic progestogen widely prescribed for the management of progesterone deficiency-related conditions. It is commonly used to regulate menstrual cycles, support early pregnancy, and manage various gynecological disorders.

By closely mimicking the action of natural progesterone, AFTERGEST helps restore hormonal balance, maintain endometrial stability, and improve reproductive health—enhancing overall well-being and quality of life for women.

Manufactured in a WHO-GMP, USFDA, and EUGMP-certified facility, AFTERGEST ensures high purity, consistent quality, optimal bioavailability, and excellent patient compliance—making it ideal for PCD Pharma Franchise, third-party manufacturing, and export markets.

Dydrogesterone acts selectively on progesterone receptors in the uterus and reproductive tissues.

• Promotes proper endometrial development

• Regulates menstrual cycle patterns

• Supports implantation and early pregnancy

• Reduces risk of progesterone-deficiency-related miscarriage (as prescribed)

• Balances estrogen effects in hormone therapy

It provides targeted progesterone support with minimal androgenic or estrogenic side effects, ensuring better tolerability.

✅ Clinically proven progesterone replacement therapy
✅ Effective in menstrual irregularities & luteal phase defects
✅ Supports early pregnancy maintenance
✅ Useful in infertility treatment protocols
✅ Helps manage endometriosis & dysfunctional uterine bleeding
✅ Favorable safety and tolerability profile
✅ Manufactured in WHO-GMP & USFDA-certified facilities
✅ EUGMP-compliant for regulated export markets
✅ PCD Pharma Franchise & third-party manufacturing ready
✅ High-quality blister packaging for enhanced stability

✔️ Threatened miscarriage (as prescribed)
✔️ Recurrent pregnancy loss due to progesterone deficiency
✔️ Luteal phase defect
✔️ Irregular menstruation
✔️ Dysmenorrhea
✔️ Endometriosis
✔️ Dysfunctional uterine bleeding
✔️ Hormone Replacement Therapy (with estrogen)
✔️ Infertility associated with progesterone deficiency

Dose: As prescribed by the gynecologist

• Usually taken once or twice daily depending on indication

• Dosage and duration vary according to clinical condition

• Should be taken regularly at the same time each day

• Headache

• Nausea

• Breast tenderness

• Mild abdominal discomfort

• Temporary spotting or breakthrough bleeding

✅ High-purity API with strict quality standards
✅ Clinically established and globally accepted molecule
✅ Minimal hormonal adverse effects
✅ Manufactured under stringent GMP compliance
✅ Suitable for domestic and international markets

✔️ PCD Pharma Franchise for gynecology range
✔️ Third-party manufacturing of Dydrogesterone Tablets
✔️ WHO-GMP certified hormone manufacturer
✔️ USFDA & EUGMP approved women’s health medicines for export

Additional Information:

• Production Capacity: Fully automated, ISO & USFDA-compliant 600,000 Sq. ft. plant with zero liquid & gas discharge facility
• Delivery Time: 45-60 DAYS
• Packaging Details: Our packaging is designed to ensure maximum product safety, stability, and market appeal. We utilize high-quality raw materials (RM) and USFDA-approved packaging components, making our products ideal for export and third-party manufacturing. Key Features of Our Packaging: ✅ Attractive & Market-Differentiating Designs: Our products come with customizable branding and change parts, allowing businesses to create a distinct identity in the pharma market. ✅ Pharmaceutical-Grade Materials: We use high-density PET bottles, tamper-evident caps, and premium blister foils to maintain product integrity. ✅ Advanced Protection: Our packaging is moisture-resistant, UV-protected, and oxidation-resistant, ensuring longer shelf life and stability. ✅ High-Precision Batch Coding & Labeling: We use laser batch coding, holographic labels, and serialized QR codes for authenticity and traceability. ✅ International Standards for Export: All our packaging materials meet USFDA, EUGMP, and WHO-GMP regulations, ensuring global compliance. Our packaging solutions help PCD Pharma companies, third-party manufacturers, and exporters differentiate their products in highly competitive markets while maintaining the highest pharmaceutical standards.

TORSEPOD-40 contains Torsemide 40 mg, a potent loop diuretic indicated for the management of moderate to severe edema and fluid retention associated with cardiac, renal, and hepatic conditions. It ensures effective and sustained removal of excess fluid, helping reduce swelling and related complications.

Manufactured in a WHO-GMP compliant facility, TORSEPOD-40 maintains high standards of quality, safety, and consistency for domestic as well as export markets.

Torsemide acts on the Loop of Henle in the kidneys to:

• Increase excretion of sodium and water

• Promote rapid and effective fluid removal

• Reduce blood volume

• Decrease cardiac workload

• Provide symptomatic relief in fluid overload conditions

Its strong and sustained diuretic action makes it suitable for once-daily dosing in many patients, as prescribed by a healthcare professional.

✔ Effective management of moderate to severe edema
✔ Potent and sustained diuretic action
✔ Helps reduce swelling and discomfort
✔ Supports improved cardiovascular and renal function
✔ Reliable fluid control in chronic conditions
✔ Manufactured under strict WHO-GMP quality standards
✔ Suitable for PCD Pharma Franchise & Third-Party Manufacturing

• Edema associated with Congestive Heart Failure

• Renal disease-related fluid retention

• Hepatic cirrhosis-associated edema

• Hypertension (as prescribed by a physician)

To be used strictly under medical supervision.

Generally well tolerated when used appropriately. Some patients may experience:

• Increased urination

• Mild dizziness or weakness

• Electrolyte imbalance (rare)

• Muscle cramps

Regular monitoring of electrolytes and kidney function is recommended during therapy, especially at higher doses.

• High-quality API procurement

• Strict in-process and finished product quality testing

• Advanced blister packaging for enhanced stability and shelf life

• Complete technical documentation support

• Suitable for domestic distribution and export markets

Dosage and duration should be determined by a qualified healthcare professional based on the patient’s clinical condition and response to therapy. Regular monitoring is advised to ensure safe and effective treatment.

VSOOTH is a scientifically formulated Lactic Acid 1.2% w/v Antiseptic Vaginal Wash, designed to maintain intimate hygiene and support natural vaginal pH balance. It helps protect against irritation, unpleasant odor, and microbial overgrowth while preserving the normal vaginal flora.

Manufactured in a WHO-GMP compliant facility using high-quality active ingredients and gynecologically tested excipients, VSOOTH ensures optimal safety, gentle cleansing, and superior patient compliance — making it suitable for PCD Pharma Franchise, third-party manufacturing, and export markets.

Lactic Acid (1.2% w/v):
Lactic Acid helps maintain the natural acidic pH of the vaginal environment (typically between 3.5–4.5). An acidic pH inhibits the growth of harmful bacteria and supports the proliferation of protective lactobacilli.

By restoring and maintaining physiological pH levels, VSOOTH helps prevent infections, control odor, and reduce irritation.

The gentle wash base ensures mild cleansing without disrupting the natural microbial balance or causing excessive dryness.

✅ Maintains Natural Vaginal pH Balance
✅ Supports Healthy Vaginal Flora
✅ Helps Prevent Odor & Irritation
✅ Gentle & Soap-Free Cleansing Formula
✅ Suitable for Daily Intimate Hygiene
✅ Gynecologically Designed Formulation
✅ WHO-GMP Manufactured
✅ Suitable for PCD Pharma & Third-Party Manufacturing
✅ Export-Quality Standards

✔️ Women experiencing vaginal discomfort or irritation
✔️ Individuals prone to recurrent vaginal infections
✔️ For maintaining daily intimate hygiene
✔️ During menstruation for added freshness
✔️ Post-gynecological procedures (as advised by physician)
✔️ Gynecology clinics, hospitals & healthcare providers
✔️ Pharmacies, distributors, stockists & international buyers

Mild temporary irritation
Slight burning sensation (initial use)
Allergic reaction in hypersensitive individuals

⚠️ For external use only. Do not use internally. Discontinue use if irritation persists. Consult a healthcare professional before use during pregnancy or in case of active infection.

Additional Information:

• Production Capacity: Fully automated, ISO & USFDA-compliant 600,000 Sq. ft. plant with zero liquid & gas discharge facility
• Delivery Time: 45-60 days
• Packaging Details: Our packaging is designed to ensure maximum product safety, stability, and market appeal. We utilize high-quality raw materials (RM) and USFDA-approved packaging components, making our products ideal for export and third-party manufacturing. Key Features of Our Packaging: ✅ Attractive & Market-Differentiating Designs: Our products come with customizable branding and change parts, allowing businesses to create a distinct identity in the pharma market. ✅ Pharmaceutical-Grade Materials: We use high-density PET bottles, tamper-evident caps, and premium blister foils to maintain product integrity. ✅ Advanced Protection: Our packaging is moisture-resistant, UV-protected, and oxidation-resistant, ensuring longer shelf life and stability. ✅ High-Precision Batch Coding & Labeling: We use laser batch coding, holographic labels, and serialized QR codes for authenticity and traceability. ✅ International Standards for Export: All our packaging materials meet USFDA, EUGMP, and WHO-GMP regulations, ensuring global compliance. Our packaging solutions help PCD Pharma companies, third-party manufacturers, and exporters differentiate their products in highly competitive markets while maintaining the highest pharmaceutical standards.

ATERSCAB is a topical anti-parasitic cream formulated with Permethrin 5% w/v, indicated for the effective treatment of scabies and lice infestations. It is a clinically proven scabicidal agent designed to eliminate mites and their eggs with high efficacy and patient safety.

Manufactured in a WHO-GMP compliant facility using high-quality APIs and dermatologically compatible excipients, ATERSCAB ensures optimal skin coverage, enhanced therapeutic response, and improved patient compliance — making it suitable for PCD Pharma Franchise, third-party manufacturing, and export markets.

Permethrin (5% w/v):
A synthetic pyrethroid that acts on the nerve cell membranes of parasites. It disrupts sodium channel function, leading to delayed repolarization, paralysis, and eventual death of Sarcoptes scabiei mites and lice.

Permethrin is ovicidal and adulticidal, meaning it kills both live parasites and their eggs, helping prevent reinfestation when used as directed.

✅ Highly Effective Scabies Treatment
✅ Kills Mites & Their Eggs (Ovicidal Action)
✅ Rapid Relief from Itching & Skin Irritation
✅ Dermatologically Safe When Used as Directed
✅ Uniform Cream Base for Easy Application
✅ WHO-GMP Manufactured
✅ Suitable for PCD Pharma & Third-Party Manufacturing
✅ Export-Quality Standards

✔️ Patients diagnosed with scabies infestation
✔️ Individuals experiencing intense itching, especially at night
✔️ Family members or close contacts of infected persons
✔️ Patients with lice infestations (as prescribed)
✔️ Hospitals, dermatology clinics & general practitioners
✔️ Pharmacies, distributors, stockists & international buyers

Mild burning sensation
Skin redness
Temporary itching
Mild rash at application site

⚠️ For external use only. Avoid contact with eyes, mouth, and broken skin. Use under medical supervision, especially in infants, elderly patients, or pregnant women.

✅ High-Quality API & Excipients: Sourced from validated vendors ensuring purity, safety, and efficacy.
✅ Dermatologically Balanced Cream Base: Ensures uniform drug distribution and better skin adherence.
✅ Strict Quality Control: Manufactured under WHO-GMP standards with validated processes and in-process checks.
✅ Microbial & Cross-Contamination Control: Controlled production environment with stringent hygiene protocols.
✅ Premium Packaging Options: Tube packs ensuring product stability and ease of dispensing.
✅ After-Sales Technical Support: Regulatory, documentation, and marketing assistance for domestic and export markets.

✔️ PCD Pharma Franchise for Scabies Cream
✔️ Third-Party Manufacturing of Permethrin 5% Cream
✔️ Best Scabies Treatment Medicine Supplier in India
✔️ WHO-GMP Certified Anti-Scabies Cream Manufacturer
✔️ Permethrin Cream Exporter
✔️ Anti-Parasitic Medicines for Stockists & Distributors

VOMICAP DROP is a clinically effective antiemetic formulation specially designed to provide rapid relief from nausea and vomiting in infants and children. Its fast-acting mechanism helps control gastric discomfort while improving hydration tolerance and overall recovery.

Manufactured in a WHO-GMP-certified facility under stringent quality standards, VOMICAP DROP ensures high purity, accurate dosing, optimal stability, and enhanced pediatric compliance. It is ideally positioned for PCD Pharma Franchise, third-party manufacturing, and regulated export markets.

• Blocks specific receptors responsible for triggering nausea and vomiting

• Helps regulate gastric motility

• Reduces episodes of vomiting and retching

• Improves tolerance to oral fluids and food

• Helps prevent dehydration associated with vomiting

• Promotes faster recovery in gastrointestinal disturbances

• Rapid relief from nausea and vomiting

• Suitable for infants and pediatric patients (as prescribed)

• Helps manage vomiting due to infections or indigestion

• Supports improved oral intake and hydration

• Accurate dropper dosing for precise administration

• Pleasant taste for better acceptance

• WHO-GMP-certified manufacturing

• Stable, leak-proof packaging

• Ideal for domestic and export markets

• PCD Pharma Franchise & third-party manufacturing ready

• Acute nausea and vomiting

• Gastroenteritis-associated vomiting

• Drug-induced nausea (as advised by physician)

• Vomiting associated with fever or infections

• Dose: As directed by the physician

• Pediatric dosing based on age and body weight

• Use the calibrated dropper for accurate dosing

• Administer as prescribed for recommended duration

• Mild constipation or diarrhea

• Headache

• Dizziness (rare)

• Temporary gastrointestinal discomfort

• Clinically reliable antiemetic therapy

• Pediatric-friendly formulation

• High-quality API and excipients

• Strict quality assurance and contamination control

• Excellent stability and shelf life

• Strong franchise and export potential

Ideal for partners seeking:

• Pediatric antiemetic drops PCD Franchise

• Third-party manufacturing of anti-vomiting drops

• WHO-GMP-certified pediatric manufacturer

• Export-ready gastrointestinal care formulations

RUTWASH is a dermatologically formulated cleansing solution containing Salicylic Acid 2% Face Wash, designed for effective management of acne-prone, oily, and blemish-prone skin. It provides deep pore cleansing while gently exfoliating dead skin cells to promote clearer and healthier skin.

Manufactured in a WHO-GMP compliant facility using high-quality active ingredients and skin-compatible excipients, RUTWASH ensures optimal cleansing efficiency, controlled exfoliation, and enhanced patient compliance — making it suitable for PCD Pharma Franchise, third-party manufacturing, and export markets.

Salicylic Acid (2%):
A beta-hydroxy acid (BHA) that penetrates deep into pores to dissolve excess sebum, debris, and dead skin cells. It works through keratolytic action, promoting exfoliation and preventing pore blockage — a key factor in acne formation.

Salicylic Acid also exhibits mild anti-inflammatory properties, helping reduce redness, swelling, and irritation associated with acne lesions.

The face wash base ensures gentle cleansing without excessive dryness, maintaining skin balance while controlling oil production.

✅ Deep Pore Cleansing Action
✅ Helps Reduce Acne & Blackheads
✅ Controls Excess Oil Secretion
✅ Promotes Gentle Exfoliation
✅ Reduces Acne-Related Inflammation
✅ Non-Comedogenic & Dermatologically Designed
✅ WHO-GMP Manufactured
✅ Suitable for PCD Pharma & Third-Party Manufacturing
✅ Export-Quality Standards

✔️ Individuals with oily and acne-prone skin
✔️ Patients experiencing blackheads and whiteheads
✔️ Mild to moderate acne management
✔️ Teenagers and adults with frequent breakouts
✔️ Dermatology clinics & skincare specialists
✔️ Pharmacies, distributors, stockists & international buyers

Mild dryness
Skin peeling
Temporary redness
Mild stinging sensation

⚠️ For external use only. Avoid contact with eyes. Use sunscreen during daytime as Salicylic Acid may increase skin sensitivity to sunlight. Consult a healthcare professional if irritation persists.

✅ High-Quality Active & Excipients: Sourced from validated vendors ensuring purity and safety.
✅ Balanced Cleansing Base: Provides effective exfoliation without over-drying the skin.
✅ Strict Quality Control: Manufactured under WHO-GMP standards with validated production processes.
✅ Microbial Control & Hygiene: Produced in controlled environments with stringent quality checks.
✅ Premium Packaging Options: Leak-proof, user-friendly packaging ensuring stability.
✅ After-Sales Technical Support: Complete regulatory and marketing assistance for domestic and export markets.

CAMCETA-P is a scientifically formulated combination of Camylofin Dihydrochloride 50 mg + Paracetamol 325 mg, designed to provide effective relief from abdominal spasms, colicky pain, and fever associated with gastrointestinal and gynecological conditions.

This dual-action formula works by relaxing smooth muscles while simultaneously reducing pain and discomfort, offering fast and reliable symptomatic relief.

Manufactured in a WHO-GMP compliant facility, CAMCETA-P ensures superior quality, safety, and stability — making it ideal for:

• PCD Pharma Franchise

• Third-Party Manufacturing

• Institutional Supply

• Domestic & Export Markets

• Potent antispasmodic agent

• Relaxes smooth muscles of the gastrointestinal, biliary & genitourinary tract

• Reduces painful spasms and abdominal cramping

• Provides quick relief in colicky conditions

• Well-established analgesic & antipyretic

• Reduces pain intensity

• Controls associated fever

• Enhances overall comfort when combined with antispasmodic therapy

✅ Dual-action formula for spasm + pain relief
✅ Effective in abdominal colic & GI spasms
✅ Helpful in dysmenorrhea (menstrual cramps)
✅ Provides fast symptomatic relief
✅ Well-tolerated combination therapy
✅ Manufactured in WHO-GMP compliant facility
✅ Ideal for PCD & third-party manufacturing
✅ Stable blister packaging for better shelf life
✅ Suitable for domestic & export markets

✔ Patients with abdominal colic & spasmodic pain
✔ Individuals suffering from gastrointestinal cramps
✔ Women experiencing menstrual cramps
✔ Supportive therapy in biliary or renal colic
✔ Suitable for wholesalers, stockists & distributors

(Use under medical supervision.)

• Mild nausea

• Gastric discomfort

• Dizziness

• Rare hypersensitivity reactions

Caution in patients with liver disorders due to Paracetamol component.

✅ Quality Raw Materials: Pharmacopeial-grade APIs & validated excipients
✅ Advanced Manufacturing: WHO-GMP compliant facility with strict QC protocols
✅ Microbial & Cross-Contamination Control: Controlled production environment
✅ Superior Packaging: Blister/Alu-Alu options for enhanced stability
✅ Technical & Marketing Support: Assistance for franchise partners & distributors

✔ PCD Pharma Franchise – Gastro & Pain Segment
✔ Third-Party Manufacturing of Camylofin + Paracetamol Tablets
✔ Reliable Antispasmodic & Analgesic Tablet Supplier
✔ WHO-GMP Certified Pain & GI Care Manufacturer
✔ Export-Quality Spasm Relief Tablets
✔ Gastro & Women’s Health Products for Stockists

Additional Information:

• Production Capacity: Fully automated, ISO & USFDA-compliant 600,000 Sq. ft. plant with zero liquid & gas discharge facility
• Delivery Time: 45-60 DAYS
• Packaging Details: Our packaging is designed to ensure maximum product safety, stability, and market appeal. We utilize high-quality raw materials (RM) and USFDA-approved packaging components, making our products ideal for export and third-party manufacturing. Key Features of Our Packaging: ✅ Attractive & Market-Differentiating Designs: Our products come with customizable branding and change parts, allowing businesses to create a distinct identity in the pharma market. ✅ Pharmaceutical-Grade Materials: We use high-density PET bottles, tamper-evident caps, and premium blister foils to maintain product integrity. ✅ Advanced Protection: Our packaging is moisture-resistant, UV-protected, and oxidation-resistant, ensuring longer shelf life and stability. ✅ High-Precision Batch Coding & Labeling: We use laser batch coding, holographic labels, and serialized QR codes for authenticity and traceability. ✅ International Standards for Export: All our packaging materials meet USFDA, EUGMP, and WHO-GMP regulations, ensuring global compliance. Our packaging solutions help PCD Pharma companies, third-party manufacturers, and exporters differentiate their products in highly competitive markets while maintaining the highest pharmaceutical standards.

Polyethylene Glycol 3350 USP (PEG 3350) is a widely prescribed osmotic laxative used for the treatment of occasional constipation and bowel irregularity. It works by retaining water in the stool, making it softer and easier to pass without causing harsh stimulation of the intestines.

Manufactured in WHO-GMP compliant facilities following stringent quality standards, Polyethylene Glycol 3350 USP ensures high purity, consistent particle size, optimal solubility, and reliable therapeutic outcomes. It is ideal for domestic markets, PCD Pharma Franchise, third-party manufacturing, and export opportunities.

• Osmotic agent that binds water in the colon

• Increases water content of stool

• Softens stool for easy passage

• Promotes comfortable bowel movements

• Non-stimulant action reduces cramping

PEG 3350 is minimally absorbed in the body, making it safe for regular use under medical supervision.

✅ Gentle and effective constipation relief
✅ Non-habit forming when used as directed
✅ Softens stool naturally
✅ Minimal systemic absorption
✅ Suitable for short-term and physician-guided long-term use
✅ Palatable and easy-to-mix powder formulation
✅ USP-grade quality assurance
✅ Manufactured under strict GMP standards
✅ Suitable for PCD & third-party manufacturing

✔️ Occasional constipation
✔️ Chronic constipation (as advised by physician)
✔️ Bowel regulation therapy
✔️ Pre-procedural bowel preparation (in higher doses under medical supervision)
✔️ Constipation associated with lifestyle or dietary changes

Dose: As directed by the physician

• Typically dissolved in water or any preferred beverage

• Usually taken once daily

• Ensure adequate fluid intake

• Effects generally seen within 24–72 hours

Do not exceed recommended dosage without medical advice.

Polyethylene Glycol 3350 is generally well tolerated.

• Bloating

• Flatulence

• Nausea

• Mild abdominal discomfort

Serious side effects are rare when used appropriately.

✅ USP-grade raw material for superior purity
✅ Consistent particle size for better solubility
✅ Clinically trusted osmotic laxative
✅ Suitable for pediatric, adult, and geriatric populations (as prescribed)
✅ High demand in gastro and general practice
✅ Strong commercial viability
✅ Export-ready documentation support

• Moisture-resistant sachets

• HDPE containers with measuring cap

• Custom private labeling available

• Long shelf-life stability

✔️ PCD Pharma Franchise for gastro range
✔️ Third-party manufacturing of PEG 3350 powder
✔️ WHO-GMP certified laxative manufacturer
✔️ Export-quality bowel regulation products

• Store in a cool, dry place

• Protect from moisture

• Keep container tightly closed

• Keep out of reach of children

Polyethylene Glycol 3350 USP offers safe, effective, and gentle relief from constipation with excellent tolerability and strong clinical acceptance. Backed by high-quality manufacturing standards and growing market demand, it is a valuable addition to gastrointestinal product portfolios with significant commercial potential.

Additional Information:

• Production Capacity: Fully automated, ISO & USFDA-compliant 600,000 Sq. ft. plant with zero liquid & gas discharge facility
• Delivery Time: 45-60 DAYS
• Packaging Details: Our packaging is designed to ensure maximum product safety, stability, and market appeal. We utilize high-quality raw materials (RM) and USFDA-approved packaging components, making our products ideal for export and third-party manufacturing. Key Features of Our Packaging: ✅ Attractive & Market-Differentiating Designs: Our products come with customizable branding and change parts, allowing businesses to create a distinct identity in the pharma market. ✅ Pharmaceutical-Grade Materials: We use high-density PET bottles, tamper-evident caps, and premium blister foils to maintain product integrity. ✅ Advanced Protection: Our packaging is moisture-resistant, UV-protected, and oxidation-resistant, ensuring longer shelf life and stability. ✅ High-Precision Batch Coding & Labeling: We use laser batch coding, holographic labels, and serialized QR codes for authenticity and traceability. ✅ International Standards for Export: All our packaging materials meet USFDA, EUGMP, and WHO-GMP regulations, ensuring global compliance. Our packaging solutions help PCD Pharma companies, third-party manufacturers, and exporters differentiate their products in highly competitive markets while maintaining the highest pharmaceutical standards.