Biofield Pharma Private Limited

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.

How Does It Work?

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.

Key Features & Benefits

✅ 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

Indications

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

Dosage & Administration

Dose: As prescribed by the physician

Usually taken after meals

Follow healthcare professional’s advice for safe and effective use

Side Effects (Usually Mild & Rare)

Mild nausea

Dizziness

Dry mouth

Allergic reactions (rare)

(Use under medical supervision.)

Why Choose AFTERSPAS-P?

✅ 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

Customers Looking For

✔️ 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.

NASOWIPE – Xylometazoline 0.1% + Benzalkonium Chloride 0.02%

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

Composition (per mL)

• Xylometazoline 1 mg – nasal decongestant

• Benzalkonium Chloride 0.2 mg – preservative

• Sterile water q.s.

Mechanism of Action

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

• Benzalkonium Chloride: Preservative; mild antiseptic

Indications

• Nasal congestion: common cold, allergic rhinitis, sinusitis

• Pre-nasal examination or minor procedures

Dosage

• 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

Contraindications

• Hypersensitivity to Xylometazoline or Benzalkonium Chloride

• Severe hypertension, heart disease, glaucoma

• MAO inhibitor use

Precautions

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

• Avoid in children <6 yrs without doctor guidance

• Caution in cardiovascular disorders

Adverse Effects

• Mild stinging, burning, dryness

• Rare: sneezing, headache, rebound congestion, palpitations

Storage

• Store below 25°C, protect from light

• Keep bottle closed; discard 4 weeks after opening

Summary

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.

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.

How It Works Antiemetic Action

• Blocks specific receptors responsible for triggering nausea and vomiting

• Helps regulate gastric motility

• Reduces episodes of vomiting and retching

Gastrointestinal Comfort Support

• Improves tolerance to oral fluids and food

• Helps prevent dehydration associated with vomiting

• Promotes faster recovery in gastrointestinal disturbances

Key Features & Benefits

• 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

Indications

• Acute nausea and vomiting

• Gastroenteritis-associated vomiting

• Drug-induced nausea (as advised by physician)

• Vomiting associated with fever or infections

Dosage & Administration

• 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

Possible Side Effects (Generally Mild)

• Mild constipation or diarrhea

• Headache

• Dizziness (rare)

• Temporary gastrointestinal discomfort

Why Choose VOMICAP DROP?

• 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

Business Opportunities

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

HEXICO – Chlorhexidine Gluconate 0.2% + Sodium Benzoate 0.02% Mouthwash

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

Composition (per 100 mL)

• Chlorhexidine Gluconate 0.2% – active antiseptic

• Sodium Benzoate 0.02% – preservative

• Purified water q.s.

Mechanism of Action

• Chlorhexidine: Disrupts bacterial cell membranes → bactericidal

• Sodium Benzoate: Preservative; maintains sterility

Indications

• Gingivitis, periodontitis

• Plaque control

• Post-dental surgery oral hygiene

• Oral infections prevention

Dosage & Administration

• 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

Contraindications

• Allergy to Chlorhexidine or preservatives

Precautions

• Topical use only; avoid swallowing

• Short-term use to prevent mucosal irritation

• May stain teeth/tongue; avoid anionic toothpaste concurrently

Adverse Effects

• Temporary burning, altered taste

• Rare: oral irritation, allergy, staining

Storage

• Store 2–25°C, protect from light

• Keep bottle closed; discard after 6 months of opening

Summary

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.

AFTERAX-10 is a clinically effective anti-allergic formulation designed to provide rapid and sustained relief from allergic conditions and associated itching. It helps control hypersensitivity reactions while improving patient comfort and quality of life.

Manufactured in a WHO-GMP-certified facility under stringent quality control systems, AFTERAX-10 ensures high purity, optimal bioavailability, and consistent therapeutic performance. The product is ideally positioned for PCD Pharma Franchise, third-party manufacturing, and regulated export markets.

How It Works Antihistaminic Action

• Blocks histamine (H1) receptors responsible for allergic symptoms

• Reduces itching, redness, swelling, and skin irritation

• Controls sneezing, watery eyes, and runny nose

Anti-Pruritic Effect

• Provides effective relief from skin itching and rashes

• Helps calm hypersensitive skin reactions

• Improves comfort in acute and chronic allergic conditions

Key Features & Benefits

• Effective relief from allergic rhinitis and urticaria

• Reduces itching, redness, and skin irritation

• Controls sneezing and watery nasal discharge

• Suitable for acute and chronic allergy management

• Once or twice daily dosing (as prescribed)

• High-quality API and excipients

• WHO-GMP-certified manufacturing standards

• Stable packaging for extended shelf life

• Ideal for domestic and export markets

• PCD Pharma Franchise & third-party manufacturing ready

Indications

• Allergic rhinitis

• Urticaria (hives)

• Skin allergies and rashes

• Pruritus (itching)

• Hypersensitivity reactions

Dosage & Administration

• Dose: As directed by the physician

• Usually administered once or twice daily

• Swallow with water

• Follow prescribed duration for best results

Possible Side Effects (Generally Mild)

• Mild drowsiness (depending on formulation)

• Dry mouth

• Headache

• Gastrointestinal discomfort (rare)

Why Choose AFTERAX-10?

• Clinically trusted anti-allergic therapy

• Reliable symptom control with good tolerability

• Strict quality assurance and manufacturing compliance

• Suitable for long-term allergy management

• Strong franchise and export potential

Business Opportunities

Ideal for partners seeking:

• Anti-allergic tablet PCD Franchise

• Third-party manufacturing of antihistamine tablets

• WHO-GMP-certified allergy care manufacturer

• Export-ready anti-allergic formulations

YOLACT DROPS is a clinically formulated probiotic preparation designed to support digestive health and restore healthy gut flora in infants and children. It helps manage diarrhea, antibiotic-associated gut imbalance, colic, and digestive disturbances while promoting overall gastrointestinal wellness.

Manufactured in a WHO-GMP-certified facility under stringent quality control standards, YOLACT DROPS ensures high stability, viable probiotic count, precise dosing, and enhanced pediatric compliance. It is ideally positioned for PCD Pharma Franchise, third-party manufacturing, and regulated export markets.

How It WorksProbiotic Action

• Restores beneficial intestinal microflora

• Suppresses growth of harmful bacteria

• Maintains healthy gut balance

Digestive Support

• Improves digestion and nutrient absorption

• Reduces bloating, gas, and abdominal discomfort

• Supports faster recovery from diarrhea

Gut Immunity Enhancement

• Strengthens intestinal defense mechanisms

• Supports overall immune function in children

Key Features & Benefits

• Clinically effective probiotic formulation

• Helps manage acute and antibiotic-associated diarrhea

• Supports healthy digestion in infants and children

• Reduces colic, bloating, and gastrointestinal discomfort

• Stable formulation with maintained probiotic viability

• Easy-to-administer dropper for accurate dosing

• Pleasant taste for better acceptance

• WHO-GMP-certified manufacturing

• Leak-proof, stability-tested packaging

• Ideal for domestic and export markets

• PCD Pharma Franchise & third-party manufacturing ready

Indications

• Acute diarrhea

• Antibiotic-associated diarrhea

• Infantile colic

• Digestive imbalance

• Gastrointestinal disturbances

Dosage & Administration

• Dose: As directed by the physician

• Pediatric dosage based on age and clinical condition

• Shake well before use (if required)

• Use the calibrated dropper for accurate dosing

Possible Side Effects (Generally Rare & Mild)

• Mild bloating (initially)

• Temporary gastrointestinal discomfort

Why Choose YOLACT DROPS?

• Scientifically developed probiotic support

• High-quality strains with stable viability

• Strict quality assurance and contamination control

• Pediatric-friendly formulation

• Strong franchise and export potential

• Designed for improved gut health and immunity support

Business Opportunities

Ideal for partners seeking:

 

• Pediatric probiotic drops PCD Franchise

• Third-party manufacturing of probiotic formulations

• WHO-GMP-certified pediatric manufacturer

• Export-ready gastrointestinal care 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.

UT STONYL Crush is a clinically formulated tablet designed to support the management and prevention of urinary stones in adults. Its dual-action mechanism helps dissolve certain types of urinary calculi while promoting healthy urinary tract function and preventing recurrence.

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

How It Works Urinary Stone Dissolution

• Contains active ingredients that help reduce stone formation

• Aids in breaking down uric acid, calcium oxalate, or phosphate stones (depending on formulation)

• Helps restore normal urinary pH to prevent crystallization

Urinary Tract Support

• Promotes healthy urinary flow and bladder function

• Reduces irritation, burning, and discomfort during urination

• Supports overall kidney and urinary tract health

Key Features & Benefits

• Clinically effective in urinary stone management

• Helps dissolve certain types of urinary calculi and prevent recurrence

• Supports urinary tract health and proper kidney function

• Reduces burning, irritation, and discomfort during urination

• Adult-friendly tablet formulation 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

Indications

• Management of urinary stones (renal calculi)

• Prevention of recurrent urinary stone formation

• Supportive care for urinary tract discomfort

• Adult patients prone to urolithiasis

Dosage & Administration

• Dose: As directed by the physician

• Adult dosing based on stone type, severity, and physician’s recommendation

• Swallow whole with water

• Follow prescribed duration for optimal results

Possible Side Effects (Generally Mild)

• Mild gastrointestinal discomfort (nausea, indigestion)

• Temporary urinary frequency

• Rare allergic reactions

Why Choose UT STONYL Crush?

• Scientifically formulated tablet for urinary stone management

• Clinically proven mechanism to reduce stone formation and recurrence

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

• Strict quality assurance and manufacturing compliance

• Convenient adult-friendly tablet formulation

• Strong franchise and export potential

Business Opportunities

Ideal for partners seeking:

• Urinary stone management tablet PCD Franchise

• Third-party manufacturing of renal and urinary care formulations

• WHO-GMP-certified urinary health manufacturer

• Export-ready renal care 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.

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.

How It Works Bronchodilator Action

• Relaxes smooth muscles in the airways

• Reduces bronchospasm and airway obstruction

• Improves airflow and oxygen delivery

Anti-Inflammatory & Symptom Relief

• Helps reduce airway inflammation and mucus production

• Relieves wheezing, shortness of breath, and chest tightness

• Supports long-term management of chronic respiratory conditions

Key Features & Benefits

• 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

Indications

• Bronchial asthma

• Chronic obstructive pulmonary disease (COPD)

• Bronchitis and wheezing disorders

• Allergic respiratory conditions

• Shortness of breath and bronchospasm management

Dosage & Administration

• 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

Possible Side Effects (Generally Mild)

• Mild tremors or palpitations

• Headache or dizziness

• Gastrointestinal discomfort (nausea, upset stomach)

• Rare hypersensitivity reactions

Why Choose VENTAWAY?

• 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

Business Opportunities

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.

BACILO RITE is a clinically proven probiotic formulation containing Bacillus clausii spores 2 Billion CFU, specially designed to restore and maintain healthy intestinal microflora. It is widely prescribed for the management of antibiotic-associated diarrhea, acute and chronic diarrhea, intestinal dysbiosis, and gastrointestinal disturbances. As a spore-forming probiotic, it survives gastric acidity and ensures effective gut colonization.

Manufactured in a WHO-GMP, USFDA, and EUGMP-certified facility, BACILO RITE assures high purity, stability, and superior efficacy, making it ideal for PCD Pharma Franchise, third-party manufacturing, and export markets.

How Does It Work?

Bacillus clausii Spores (2 Billion CFU):

• Restores normal intestinal flora disrupted by antibiotics or infections

• Inhibits growth of harmful pathogenic bacteria

• Produces antimicrobial substances supporting gut health

• Enhances intestinal immunity and digestion

• Improves nutrient absorption and gut balance

Key Features & Benefits

✅ Clinically proven probiotic for gut health
✅ Effective in antibiotic-associated & infectious diarrhea
✅ Restores and maintains healthy gut microflora
✅ Resistant to antibiotics and gastric acid
✅ Improves digestion and intestinal immunity
✅ Safe for children, adults, and elderly
✅ Manufactured in WHO-GMP & USFDA-certified facilities
✅ EUGMP-compliant for regulated export markets
✅ PCD Pharma Franchise & third-party manufacturing ready
✅ Stable, leak-proof packaging ensures longer shelf life

Indications

✔️ Antibiotic-associated diarrhea
✔️ Acute & chronic diarrhea
✔️ Gastrointestinal infections
✔️ Intestinal dysbiosis
✔️ Gut imbalance after antibiotic therapy

Dosage & Administration

• Dose: As directed by the physician

• Can be taken with or without food

• Suitable for pediatric and adult use

Side Effects (Rare & Mild)

• Mild bloating or flatulence

• Very rare hypersensitivity reactions

Why Choose BACILO RITE?

✅ High-viability Bacillus clausii spores for maximum efficacy
✅ Antibiotic-resistant probiotic strain effective during antibiotic therapy
✅ Strict quality control & contamination prevention
✅ Clinically trusted formulation with excellent patient compliance
✅ Export-quality packaging for improved stability and shelf life

Customers Looking For

✔️ PCD Pharma Franchise for probiotic & GI medicines
✔️ Third-party manufacturing of Bacillus clausii oral suspension
✔️ Best probiotic supplier in India
✔️ WHO-GMP certified probiotic manufacturer
✔️ USFDA & EUGMP approved GI 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.

AFTERCOL DS Syrup is a clinically balanced formulation designed to provide effective relief from common cold, allergic rhinitis, nasal congestion, and associated cough in children. Its multi-action approach helps control symptoms while improving breathing comfort and overall recovery.

Manufactured in a WHO-GMP-certified facility with stringent quality standards, AFTERCOL DS Syrup ensures high purity, stability, accurate dosing, and excellent palatability for better pediatric compliance. It is ideally positioned for PCD Pharma Franchise, third-party manufacturing, and regulated export markets.

How It Works Antihistamine Action

• Blocks histamine receptors to reduce sneezing and runny nose

• Controls watery eyes and nasal irritation

• Provides relief from allergic symptoms

Decongestant Action

• Reduces swelling of nasal passages

• Relieves sinus pressure and nasal blockage

• Improves airflow and breathing comfort

Cough Relief Action (As per formulation)

• Soothes throat irritation

• Suppresses dry cough or helps loosen mucus

• Promotes easier breathing and restful sleep

Key Features & Benefits

• Multi-action formula for cold, allergy, and cough relief

• Effective in seasonal and allergic rhinitis

• Reduces sneezing, nasal blockage, throat irritation & cough

• Helps relieve sinus congestion and pressure

• Pleasant taste for improved pediatric acceptance

• Accurate dosing with measuring cup

• WHO-GMP-certified manufacturing

• Stable, leak-proof packaging for extended shelf life

• Suitable for domestic and export markets

• Ideal for PCD Pharma Franchise & third-party manufacturing

Indications

• Common cold

• Allergic rhinitis

• Nasal congestion

• Sneezing and runny nose

• Cough associated with upper respiratory tract infections

Dosage & Administration

• Dose: As directed by the physician

• Pediatric dosage according to age and body weight

• Shake well before use

• Use the provided measuring cup for precise dosing

Possible Side Effects (Generally Mild)

• Mild drowsiness

• Dry mouth

• Nausea (rare)

• Mild gastrointestinal discomfort

Why Choose AFTERCOL DS Syrup?

• Scientifically balanced pediatric formulation

• High-quality API and excipients

• Strict quality control and safety standards

• Excellent taste for improved compliance

• Reliable manufacturing infrastructure

• Ready for franchise, third-party manufacturing, and export supply

Business Opportunities

Ideal for partners seeking:

• Pediatric cold & cough syrup PCD Franchise

• Third-party manufacturing of cough & cold syrups

• WHO-GMP-certified syrup manufacturer

• Export-ready pediatric respiratory 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.

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.

How it works

• 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.

Indications

• Sore throat and pharyngitis

• Gingivitis and oral infections

• Mouth ulcers

• Pre- and post-dental procedures for oral antisepsis

How to use

• 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

Precautions

• 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

Common Side Effects

• Mild oral irritation or staining of teeth (temporary)

• Rarely, allergic reactions

Key Points

• 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.

FEBUGRIP 40 Febuxostat Tablets IP 40 mg

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.

How Does It Work?

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

Key Features & Benefits

✅ 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

Indications (Who Should Use It?)

✔️ 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

Dosage & Administration

• Recommended Dose: As prescribed by the physician

• Generally administered once daily, with or without food

• Dose adjustment based on serum uric acid levels

Side Effects (Usually Mild & Rare)

• Nausea or headache

• Dizziness or fatigue

• Mild elevation of liver enzymes

• Skin rash (rare)

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

Why Choose FEBUGRIP 40?

✅ 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

Customers Looking For

✔️ 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.

NAXIGAB 150 is a clinically proven neuropathic pain management medicine formulated with Pregabalin 150 mg. It is widely prescribed for the treatment of neuropathic pain, including diabetic peripheral neuropathy, post-herpetic neuralgia, fibromyalgia, and as adjunctive therapy in partial seizures. By modulating abnormal nerve signals, it provides effective and sustained pain relief while improving patients’ quality of life.

Manufactured in a WHO-GMP, USFDA, and EUGMP-certified facility, NAXIGAB 150 ensures high purity, consistent quality, optimal bioavailability, and excellent patient compliance, making it ideal for PCD Pharma Franchise, third-party manufacturing, and export markets.

How Does It Work?

Pregabalin 150 mg binds to the α2-δ subunit of voltage-gated calcium channels in the central nervous system, reducing the release of excitatory neurotransmitters. This suppresses abnormal nerve impulses responsible for neuropathic pain, relieving burning, tingling, shooting, and stabbing pain, and helps control partial seizures when used as add-on therapy.

Key Features & Benefits

✅ Clinically proven therapy for neuropathic pain
✅ Effective in diabetic neuropathy & post-herpetic neuralgia
✅ Reduces nerve pain, tingling, burning & numbness
✅ Improves sleep quality and daily functioning
✅ Useful in fibromyalgia & seizure disorders
✅ Once or twice daily dosing improves compliance
✅ Manufactured in WHO-GMP & USFDA-certified facilities
✅ EUGMP-compliant for regulated export markets
✅ PCD Pharma Franchise & third-party manufacturing ready
✅ Alu-Alu blister packaging ensures stability & longer shelf life

Indications

✔️ Neuropathic pain conditions
✔️ Diabetic peripheral neuropathy
✔️ Post-herpetic neuralgia
✔️ Fibromyalgia
✔️ Partial seizures (adjunct therapy)

Dosage & Administration

• Dose: As prescribed by the physician

• Administered once or twice daily, with or without food

• Dose titration based on clinical response

Side Effects (Usually Mild & Rare)

• Dizziness or drowsiness

• Dry mouth

• Weight gain or peripheral edema

• Blurred vision or fatigue

Why Choose NAXIGAB 150?

✅ DMF-Grade API & premium excipients for superior safety
✅ Clinically established molecule with global acceptance
✅ Strict quality control & cross-contamination prevention
✅ Best-in-class Alu-Alu packaging for extended shelf life

Customers Looking For

✔️ PCD Pharma Franchise for neuropathic pain medicines
✔️ Third-party manufacturing of Pregabalin Capsules IP
✔️ WHO-GMP certified Pregabalin manufacturer
✔️ USFDA & EUGMP approved CNS 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.

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.

How Does It Work?

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.

Key Features & Benefits

✅ 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

Indications

✔️ 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

Dosage & Administration

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

Side Effects (Usually Mild & Rare)

• Headache

• Nausea

• Breast tenderness

• Mild abdominal discomfort

• Temporary spotting or breakthrough bleeding

Why Choose AFTERGEST?

✅ 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

Customers Looking For

✔️ 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.

OSTANU–FRAC is a clinically advanced bone-regeneration and calcium-support formulation designed to strengthen bones, accelerate fracture healing, and improve bone mineral density. It contains a scientifically balanced combination of Calcium, Vitamin D3, and supportive bone-health nutrients, making it ideal for orthopedic care, osteoporosis management, and post-fracture recovery.

This high-efficacy formulation enhances calcium absorption, promotes faster bone repair, and supports long-term skeletal strength. OSTANU–FRAC is widely recommended for patients with fractures, osteopenia, osteoporosis, and age-related bone weakness.

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

How Does It Work?

Calcium: Replenishes essential mineral levels required for strong bones and teeth, helping restore bone density and structural strength.

Vitamin D3 (Cholecalciferol): Enhances intestinal calcium absorption and ensures proper deposition of calcium into bones.

Bone-Support Nutrients (as per formulation): Assist in bone matrix formation, collagen support, and improved mineralization for faster fracture repair.

Together, this combination strengthens bone structure, reduces bone thinning, and accelerates healing in fracture cases.

Key Features & Benefits

✅ Supports Faster Fracture Healing
✅ Improves Bone Mineral Density
✅ Enhances Calcium Absorption & Utilization
✅ Helps Prevent Osteoporosis & Bone Weakness
✅ Suitable for Post-Menopausal & Elderly Patients
✅ Promotes Long-Term Skeletal Strength
✅ Manufactured in WHO-GMP & USFDA-Certified Facilities
✅ EUGMP-Compliant for Regulated Export Markets
✅ PCD Pharma & Third-Party Manufacturing Ready
✅ Premium Blister Packaging for Stability & Longer Shelf Life

Indications

✔️ Bone fractures & post-operative bone recovery
✔️ Osteoporosis & osteopenia
✔️ Calcium & Vitamin D deficiency
✔️ Age-related bone degeneration
✔️ Post-menopausal bone loss

Side Effects (Usually Mild & Rare)

Mild constipation

Bloating

Nausea

Excessive intake may cause hypercalcemia

(Use under medical supervision.)

Why Choose OSTANU–FRAC?

✅ DMF-grade raw materials for enhanced safety & efficacy
✅ Clinically trusted bone-strengthening formulation
✅ Strict quality control & contamination prevention
✅ High stability & extended shelf life
✅ Ideal for domestic & international markets

Customers Looking For

✔️ PCD Pharma Franchise for Bone & Fracture Care Tablets
✔️ Third-Party Manufacturing of Calcium & Vitamin D3 Combinations
✔️ WHO-GMP Certified Orthopedic Supplement Manufacturer
✔️ USFDA & EUGMP Approved Bone Health 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

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.

How Does It Work?

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.

Key Features & Benefits:

✅ 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

Indications (Who Should Use It?)

✔️ 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

Side Effects (Usually Mild & Rare):

Mild constipation

Bloating

Nausea

Excessive intake may cause hypercalcemia

(Use under medical supervision.)

Why Choose OSTANU-CCM?

✅ 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

Customers Looking For:

✔️ 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

OSTANU-CCM is a clinically formulated nutritional suspension designed to support bone health, growth, and overall wellness in children and adults. Its balanced combination of calcium, Vitamin D3, and essential multivitamins helps strengthen bones, improve immunity, and prevent nutritional deficiencies.

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

How It Works Calcium Support

• Provides essential calcium for bone and teeth strength

• Supports proper skeletal development in children and bone maintenance in adults

• Helps prevent osteoporosis and bone-related disorders

Vitamin D3 Action

• Enhances calcium absorption and metabolism

• Promotes bone mineralization and growth

• Supports immunity and overall metabolic health

Multivitamin Benefits

• Supplies essential vitamins for energy, immunity, and overall wellness

• Supports healthy skin, vision, and cognitive function

• Helps prevent fatigue, nutritional deficiencies, and weakness

Key Features & Benefits

• Comprehensive bone health and nutritional support

• Supports growth, immunity, and overall wellness

• Helps prevent vitamin and mineral deficiencies

• Pediatric-friendly suspension with pleasant taste

• Accurate dosing with measuring spoon or dropper

• WHO-GMP-certified manufacturing

• Stable, leak-proof packaging for extended shelf life

• Ideal for domestic and export markets

• PCD Pharma Franchise & third-party manufacturing ready

Indications

• Calcium and Vitamin D3 supplementation

• Prevention of rickets and osteomalacia in children

• Support in osteoporosis and bone health maintenance in adults

• Nutritional supplementation during growth, pregnancy, or illness recovery

• Weakness, fatigue, or vitamin-mineral deficiencies

Dosage & Administration

• Dose: As directed by the physician

• Pediatric and adult dosing based on age, health condition, and nutritional requirement

• Shake well before use

• Use the provided measuring spoon or dropper for accurate dosing

Possible Side Effects (Generally Mild)

• Mild gastrointestinal discomfort (constipation, nausea)

• Occasional loose stools

• Rare allergic reactions to components

Why Choose OSTANU-CCM?

• Scientifically balanced calcium, Vitamin D3, and multivitamin suspension

• High-quality API and excipients for safety and efficacy

• Strict quality assurance and contamination control

• Pediatric and adult-friendly formulation for better compliance

• Strong franchise and export potential

Business Opportunities

Ideal for partners seeking:

• Calcium and Vitamin D3 multivitamin suspension PCD Franchise

• Third-party manufacturing of nutritional supplements

• WHO-GMP-certified pediatric and adult supplement manufacturer

• Export-ready bone and nutritional care 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.

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.

How it works

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.

Indications

• Dentinal hypersensitivity (sensitive teeth)

• Prevention of dental caries

• Plaque control and mild gingivitis

How to use

• 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

Precautions

• 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

Common Side Effects

• Mild temporary tooth or gum irritation

• Rarely, slight taste alteration

Key Points

• 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.