Biofield Pharma Private Limited

CLIVAGO-N is a dermatological antibiotic gel formulated with Clindamycin Phosphate equivalent to Clindamycin 1% w/w + Nicotinamide 4% w/w, designed for the effective treatment of acne vulgaris and inflammatory skin conditions.

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

Clindamycin (1% w/w):
A lincosamide antibiotic that inhibits bacterial protein synthesis by binding to the 50S ribosomal subunit. It effectively reduces Propionibacterium acnes (Cutibacterium acnes) load and controls infection associated with acne lesions.

Nicotinamide (4% w/w):
A form of Vitamin B3 with potent anti-inflammatory properties. It reduces redness, swelling, and excess sebum production while improving skin barrier function.

The combination provides dual action — antibacterial control plus anti-inflammatory support — resulting in faster lesion healing and reduced recurrence.

✅ Effective for Mild to Moderate Acne
✅ Dual-Action Formula: Antibiotic + Anti-Inflammatory
✅ Reduces Pimples, Papules & Pustules
✅ Controls Excess Oil Secretion
✅ Minimizes Redness & Skin Irritation
✅ Smooth, Non-Greasy Gel Base for Better Absorption
✅ WHO-GMP Manufactured
✅ Suitable for PCD Pharma & Third-Party Manufacturing
✅ Export-Quality Standards

✔️ Patients with inflammatory acne vulgaris
✔️ Individuals with oily and acne-prone skin
✔️ Patients experiencing papular and pustular acne
✔️ Dermatology clinics and skin specialists
✔️ Pharmacies, distributors, stockists & international buyers

Mild skin dryness
Burning or stinging sensation
Skin irritation
Peeling at application site

⚠️ Use under medical supervision. Avoid contact with eyes and broken skin. Consult a healthcare professional before use, especially in sensitive skin conditions.

✅ High-Quality API & Excipients: Sourced from validated and compliant vendors ensuring purity and efficacy.
✅ Dermatologically Optimized Gel Base: Ensures uniform drug distribution and enhanced penetration.
✅ Strict Quality Control: Manufactured under WHO-GMP guidelines with validated production processes.
✅ Microbial & Contamination Control: Controlled environmental manufacturing zones.
✅ Premium Packaging Options: Tube packs ensuring stability and ease of use.
✅ After-Sales Technical Support: Dedicated team for regulatory, technical, and marketing assistance.

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.

ZEFROV-CV is a combination antibiotic used to treat various bacterial infections. It contains Faropenem, a broad-spectrum penem antibiotic, and Potassium Clavulanate, a beta-lactamase inhibitor that prevents bacteria from destroying the antibiotic.

• Faropenem kills bacteria by inhibiting cell wall synthesis.

• Clavulanate blocks beta-lactamase enzymes, enhancing Faropenem’s effectiveness against resistant bacteria.

• Respiratory tract infections (bronchitis, pneumonia, sinusitis)

• Urinary tract infections (UTIs)

• Skin and soft tissue infections

• Gynecological and mild intra-abdominal infections

• Usually 1 tablet twice daily, after meals

• Duration: 5–14 days (as prescribed)

• Nausea

• Vomiting

• Diarrhea

• Rash

• Avoid if allergic to penicillins

• Use cautiously in kidney or liver disease

• Complete the full course to prevent resistance

Summary:
ZEFROV-CV is a broad-spectrum oral antibiotic combination effective against beta-lactamase–producing bacteria and should be used only under medical supervision.

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.