Product image of Myconafine (Terbinafine Hydrochloride) supplied by GNH India

Myconafine

Active Ingredient:
Terbinafine Hydrochloride
Origin:
EU

Myconafine (Terbinafine Hydrochloride)

Terbinafine Hydrochloride, the active ingredient in Myconafine, is an allylamine antifungal presented as a topical formulation for cutaneous use. It works by inhibiting fungal cell membrane synthesis and is indicated for the treatment of superficial dermatophyte infections such as athlete’s foot, ringworm and jock itch in both adult and pediatric patients.

GNH India supplies Myconafine as a licensed, GDP‑compliant international pharmaceutical supplier, providing the product to hospitals, pharmacies and clinics across global markets with consistent quality and regulatory compliance.

Manufacturer / TM Owner

Aristo Pharma Sp. Z O.O.

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Indications & Clinical Uses

Terbinafine Hydrochloride is an allylamine antifungal indicated for the topical treatment of common superficial dermatophyte infections affecting the skin.

  • Tinea pedis (athlete’s foot): reduces itching, scaling and erythema while eradicating the dermatophyte on the feet.
  • Tinea corporis (ringworm): eliminates the characteristic ring‑shaped lesions and restores normal skin appearance on the trunk or limbs.
  • Tinea cruris (jock itch): clears fungal growth in the groin and inner thigh, relieving irritation and redness.

How It Works

  • Terbinafine Hydrochloride inhibits the fungal enzyme squalene epoxidase, a key step in the biosynthesis of ergosterol, the principal sterol of fungal cell membranes. Blockade of this pathway leads to accumulation of squalene, which is toxic to the fungus, and depletion of ergosterol, disrupting membrane integrity and causing fungal cell death. The selective inhibition spares human cells because humans do not rely on ergosterol for membrane structure.

Side Effects

Topical terbinafine may cause local skin reactions and, rarely, systemic adverse events.

Common Side Effects

  • Itching: mild to moderate sensation at the application site.
  • Burning: transient heat sensation during early treatment.
  • Redness: localized erythema around the treated area.
  • Scaling: flaking of skin as infection resolves.
  • Dryness: temporary loss of skin moisture.
  • Irritation: mild discomfort or stinging.

Serious or Rare Side Effects

  • Severe allergic reaction: hives, swelling, or difficulty breathing.
  • Stevens‑Johnson syndrome: rare severe skin blistering requiring medical attention.
  • Hepatic toxicity: abnormal liver function tests in systemic absorption cases.
  • Contact dermatitis: intense rash extending beyond application site.

Precautions & Warnings

When using Myconafine, consider the following precautions to ensure safe and effective treatment.

  • Assess liver function: evaluate baseline hepatic status in patients with liver disease.
  • Avoid use on broken skin: do not apply to open wounds or ulcerated areas.
  • Limit application area: restrict to affected sites and avoid excessive coverage.
  • Monitor for hypersensitivity: discontinue if signs of allergic reaction appear.
  • Use with caution in children: follow pediatric guidance and monitor for irritation.
  • Store at room temperature: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Terbinafine may interact with other medicines; awareness of major and moderate interactions helps prevent adverse outcomes.

Major Interactions (Avoid)

  • Itraconazole: combined use increases risk of hepatotoxicity.
  • Cimetidine: may raise terbinafine plasma concentrations.
  • Strong CYP2D6 inhibitors: can elevate terbinafine levels, enhancing toxicity.

Moderate Interactions (Monitor Closely)

  • Alcohol: concurrent consumption may stress liver function.
  • Warfarin: monitor INR as terbinafine may affect anticoagulant effect.
  • Other topical agents: simultaneous use may increase skin irritation.

Frequently Asked Questions

Myconafine contains terbinafine hydrochloride, a topical allylamine antifungal indicated for the treatment of superficial dermatophyte infections such as athlete’s foot, ringworm and jock itch. It works on the skin to eliminate the fungus causing these common conditions.

Terbinafine inhibits the fungal enzyme squalene epoxidase, blocking the synthesis of ergosterol, an essential component of fungal cell membranes. The resulting accumulation of squalene and depletion of ergosterol disrupts membrane integrity, leading to fungal cell death and clearance of the infection.

The dosage regimen for Myconafine is determined by the prescribing healthcare professional based on the type and extent of the infection, patient age, and local guidelines. Patients should follow the specific instructions provided on the prescription label and by their clinician.

Safety data for topical terbinafine in pregnancy and lactation are limited. Healthcare providers should weigh the potential benefits against any possible risks before prescribing Myconafine to pregnant or nursing individuals. Use only if clearly needed and under medical supervision.

To request Myconafine, submit an enquiry on the product page at gnhindia.com, specifying 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 and any necessary import documentation.

Compared with azole topical agents, terbinafine has a fungicidal mechanism that often results in faster clinical resolution and a lower risk of resistance. It is generally well‑tolerated and requires once‑daily application, whereas some alternatives may need multiple daily doses or longer treatment periods.

Store Myconafine at room temperature, below 25 °C, in its original container. Keep the product away from moisture, direct sunlight and heat sources. Ensure the cap is tightly closed after each use to maintain stability and potency.

Myconafine is applied topically to the affected skin area once daily, after washing and drying the region. A thin layer should be spread over the lesion and a small margin of surrounding healthy skin. The treated area is typically covered with a dressing only if directed by a clinician.

Although rare, serious adverse reactions can include severe allergic responses such as anaphylaxis, Stevens‑Johnson syndrome or toxic epidermal necrolysis, and hepatic toxicity manifested by abnormal liver enzymes. Patients should seek immediate medical attention if they experience widespread rash, blistering, swelling, difficulty breathing, or signs of liver dysfunction.

Myconafine should not be used by individuals with a known hypersensitivity to terbinafine, other allylamine antifungals, or any of the product’s excipients. It is also contraindicated on extensive broken skin, in patients with severe liver disease without medical supervision, and in anyone for whom a healthcare professional determines the risks outweigh the benefits.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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