Product image of Nizoral (Ketoconazole) supplied by GNH India

Nizoral

Active Ingredient:
Ketoconazole
Origin:
EU

Nizoral (Ketoconazole)

Ketoconazole, the active ingredient in Nizoral, is an imidazole antifungal presented as a topical formulation for cutaneous use. It is applied to the skin to treat superficial fungal infections such as tinea corporis, tinea cruris, tinea versicolor, and seborrheic dermatitis in adults and children.

GNH India supplies Nizoral as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, with established quality‑assurance processes and regulatory compliance across EU and other markets. Our distribution network ensures timely delivery and product integrity.

Manufacturer / TM Owner

Eurogenerics N.V./S.A.

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Indications & Clinical Uses

Ketoconazole is used topically to treat dermatophyte and yeast infections of the skin.

  • Tinea corporis: reduces fungal growth and clears the rash.
  • Tinea cruris: eliminates the causative fungus and relieves itching.
  • Tinea versicolor (pityriasis versicolor): restores normal skin pigmentation by eradicating Malassezia species.
  • Seborrheic dermatitis: controls yeast overgrowth and diminishes scaling.
  • Other superficial fungal skin infections: provides broad‑spectrum antifungal activity for various cutaneous mycoses.

How It Works

  • Ketoconazole inhibits the fungal enzyme lanosterol 14α‑demethylase, a key component of the ergosterol biosynthesis pathway. By blocking ergosterol production, it disrupts the integrity of the fungal cell membrane, leading to increased permeability and ultimately cell death. This targeted action limits fungal proliferation on the skin surface.

Side Effects

Ketoconazole is generally well tolerated when applied to intact skin, but local reactions can occur.

Common Side Effects

  • Burning sensation: mild to moderate discomfort at the application site.
  • Itching: transient pruritus during early treatment.
  • Redness: localized erythema around the treated area.
  • Dryness: skin may become less hydrated.
  • Peeling: superficial desquamation as the infection clears.

Serious or Rare Side Effects

  • Severe allergic reaction: swelling, hives, or difficulty breathing.
  • Contact dermatitis: intense inflammation requiring medical attention.
  • Skin discoloration: persistent pigment changes.
  • Secondary bacterial infection: signs of pus or worsening redness.
  • Systemic absorption leading to hepatotoxicity: extremely rare with topical use.

Precautions & Warnings

Before using ketoconazole topical products, consider the following safety measures.

  • Avoid application on broken or inflamed skin: may increase systemic absorption.
  • Do not use on extensive body surface areas without medical supervision.
  • Limit use in patients with known hypersensitivity to imidazoles.
  • Monitor for signs of allergic reaction, especially during the first week.
  • Keep the product away from eyes, mucous membranes, and genital area unless directed.
  • Store at room temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Ketoconazole topical can interact with other agents applied to the skin or taken systemically.

Major Interactions (Avoid)

  • Concurrent oral ketoconazole therapy: combined systemic exposure may increase risk of hepatotoxicity.
  • Use with other potent topical corticosteroids: may enhance systemic absorption and suppress adrenal function.

Moderate Interactions (Monitor Closely)

  • Co‑application with other antifungal creams: may cause irritation or reduce efficacy.
  • Use with occlusive dressings: can increase drug penetration and local irritation.
  • Interaction with photosensitizing agents: may heighten risk of sunburn on treated areas.

Frequently Asked Questions

Nizoral is a topical antifungal indicated for superficial fungal skin infections such as tinea corporis (ringworm), tinea cruris (jock itch), tinea versicolor (pityriasis versicolor), seborrheic dermatitis, and other dermatophyte or yeast‑related skin conditions.

Ketoconazole blocks the fungal enzyme lanosterol 14α‑demethylase, which is essential for synthesising ergosterol, a key component of the fungal cell membrane. Inhibiting this pathway disrupts membrane integrity, leading to fungal cell death and clearance of the infection.

The specific amount, frequency, and duration of Nizoral application are determined by the prescribing healthcare professional based on the infection type, severity, patient age, and treatment guidelines. Patients should follow the prescriber’s instructions precisely.

Safety data for topical ketoconazole in pregnancy and lactation are limited. Healthcare providers usually weigh the benefits against potential risks before prescribing. Women who are pregnant, planning pregnancy, or breastfeeding should discuss alternatives or precautions with their clinician.

To request Nizoral, 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 required import documentation.

Nizoral (ketoconazole) belongs to the imidazole class and offers broad‑spectrum activity against dermatophytes and yeasts. Compared with allylamine agents such as terbinafine, ketoconazole may be preferred for infections where yeast overgrowth is prominent, but individual response and tolerability guide the final choice.

Nizoral should be stored at room temperature, ideally below 25 °C, in its original packaging. Protect the product from excess moisture, direct sunlight, and extreme temperatures to maintain stability and potency.

The medication is applied to clean, dry skin in a thin layer, usually once or twice daily as directed by the prescriber. The area should be gently massaged until the product is absorbed, and hands washed after application.

Although rare, serious adverse events can include severe allergic reactions such as anaphylaxis, extensive contact dermatitis, and, in exceptional cases, systemic toxicity leading to liver enzyme abnormalities. Patients should seek immediate medical attention if they experience swelling, difficulty breathing, or intense skin reactions.

Individuals with a known hypersensitivity to ketoconazole, other imidazole antifungals, or any component of the formulation should avoid using Nizoral. It is also contraindicated on severely damaged or inflamed skin unless specifically advised by a healthcare professional.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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