Product image of Nagel Batrafen (Ciclopirox) supplied by GNH India

Nagel Batrafen

Active Ingredient:
Ciclopirox
Origin:
EU

Nagel Batrafen (Ciclopirox)

Ciclopirox, the active ingredient in Nagel Batrafen, is an antifungal presented as a topical formulation for skin use. It treats superficial fungal infections such as athlete’s foot, ringworm, jock itch and nail fungus in both adults and children, helping to eliminate the causative organisms and relieve associated symptoms.

GNH India supplies Nagel Batrafen as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company follows stringent quality standards and provides regulatory documentation to support global distribution.

Manufacturer / TM Owner

Zentiva Pharma Gmbh

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Indications & Clinical Uses

Ciclopirox is used to treat superficial fungal infections of the skin and nails.

  • Tinea pedis: reduces fungal growth and relieves itching, scaling and redness associated with athlete’s foot.
  • Tinea corporis: clears ring-shaped lesions caused by dermatophytes on the body.
  • Tinea cruris: alleviates jock itch symptoms by eradicating the responsible fungi.
  • Onychomycosis: penetrates the nail plate to eliminate fungal infection of the toenails or fingernails.
  • Other superficial fungal skin infections: effective against various yeast and mold species causing cutaneous mycoses.

How It Works

  • Ciclopirox exerts its antifungal activity by chelating intracellular metal ions, thereby inhibiting the synthesis of sterols essential for fungal cell membrane integrity. The disruption of sterol production compromises membrane function, leading to increased permeability, loss of cellular contents and ultimately fungal cell death. This broad‑spectrum action affects dermatophytes, yeasts and some molds. By targeting a pathway distinct from azole agents, ciclopirox provides an alternative mechanism for resistant strains.

Side Effects

Topical application of ciclopirox may be associated with local skin reactions.

Common Side Effects

  • Burning sensation: mild transient feeling of heat at the application site.
  • Itching: occasional pruritus during treatment.
  • Redness: localized erythema around the treated area.
  • Dryness: skin may become dry or flaky.
  • Scaling: slight flaking of the skin surface.
  • Stinging: brief sharp discomfort upon application.

Serious or Rare Side Effects

  • Allergic contact dermatitis: severe rash, swelling or blistering requiring medical attention.
  • Extensive skin irritation: intense inflammation beyond the treated area.
  • Swelling of the face or lips: signs of systemic hypersensitivity.
  • Blister formation: fluid‑filled lesions at the site of application.
  • Rare systemic effects: hepatic dysfunction reported in isolated cases.

Precautions & Warnings

When using ciclopirox topical preparations, several precautions should be observed to ensure safety and effectiveness.

  • Avoid use on broken skin: do not apply to open wounds or erosions to prevent irritation.
  • Do not apply near eyes or mucous membranes: contact may cause severe discomfort.
  • Consult healthcare professional if pregnant or breastfeeding: safety data are limited.
  • Discontinue if severe irritation occurs: seek medical advice for worsening reactions.
  • Wash hands after application: prevent accidental transfer to eyes or other body parts.
  • Store at room temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

Ciclopirox topical therapy has a low potential for systemic drug interactions, but certain combinations may affect tolerability or efficacy.

Major Interactions (Avoid)

  • Concurrent use with other topical antifungals: may increase local irritation.
  • Application over corticosteroid creams: can reduce antifungal effectiveness.

Moderate Interactions (Monitor Closely)

  • Use with skin irritants (e.g., chemical peels): monitor for enhanced irritation.
  • Combination with systemic antifungal agents: assess for overlapping toxicity.
  • Co‑application with moisturizers containing alcohol: may affect drug absorption.

Frequently Asked Questions

Nagel Batrafen contains ciclopirox and is indicated for the topical treatment of superficial fungal infections such as athlete’s foot (tinea pedis), body ringworm (tinea corporis), jock itch (tinea cruris), nail fungus (onychomycosis) and other cutaneous mycoses caused by dermatophytes, yeasts or molds.

Ciclopirox interferes with fungal cell metabolism by chelating metal ions needed for sterol synthesis. This blocks the production of essential membrane sterols, disrupting cell membrane integrity, increasing permeability and ultimately causing fungal cell death. Its mechanism differs from azole agents, offering activity against resistant strains.

The dosage regimen for Nagel Batrafen is determined by the prescribing healthcare professional. Typically, a thin layer is applied to the affected area once or twice daily, but the exact frequency, amount and duration depend on the specific infection, patient age and clinical response.

Safety data for ciclopirox topical use in pregnancy and lactation are limited. Healthcare providers should evaluate the potential benefits against any possible risks before prescribing to pregnant or nursing individuals, and patients should discuss their situation with a qualified professional.

To request Nagel Batrafen, submit an enquiry on the product page at gnhindia.com indicating the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including any cold‑chain requirements) and necessary import documentation.

Compared with azole or allylamine topical agents, ciclopirox offers a distinct mechanism by targeting sterol synthesis through metal‑ion chelation. This can be advantageous for strains resistant to azoles. However, it may be less potent than terbinafine for certain dermatophyte infections, and the choice depends on the pathogen, site of infection and patient tolerance.

Nagel Batrafen should be stored at room temperature, preferably below 25 °C. Keep the product in its original packaging, protect it from moisture, direct sunlight and extreme heat. Do not freeze the preparation, and ensure the container is tightly closed when not in use.

The medication is applied topically to clean, dry skin. A thin film is spread over the affected area and gently rubbed in. Hands should be washed after application, and the treated area should not be covered with occlusive dressings unless directed by a healthcare professional.

Serious adverse reactions, though rare, include allergic contact dermatitis, extensive skin irritation, facial or lip swelling indicating systemic hypersensitivity, and blister formation. In isolated cases, systemic absorption has been linked to hepatic dysfunction. Patients should seek immediate medical attention if they experience severe rash, swelling or systemic symptoms.

Nagel Batrafen should not be used on broken or severely inflamed skin, near the eyes or mucous membranes, or on individuals with known hypersensitivity to ciclopirox or any formulation excipients. Persons with severe liver disease should consult a physician before use, and pregnant or breastfeeding women should only use it if clearly recommended by a healthcare provider.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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