Product image of Ketoconazol Double-E Pharma (Ketoconazole) supplied by GNH India

Ketoconazol Double-E Pharma

Active Ingredient:
Ketoconazole
Origin:
EU

Ketoconazol Double-E Pharma (Ketoconazole)

Ketoconazole, the active ingredient in Ketoconazol Double-E Pharma, is an azole antifungal presented as a topical preparation for skin use. It treats fungal skin infections such as athlete's foot, ringworm and seborrheic dermatitis by targeting the causative organisms on the skin surface.

GNH India supplies Ketoconazol Double-E Pharma as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Double-E Pharma Ltd

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Indications & Clinical Uses

Ketoconazole acts on fungal pathogens that affect the skin and related structures. It is indicated for the following conditions:

  • Tinea corporis: clears ring‑shaped lesions and reduces fungal proliferation.
  • Tinea pedis: alleviates itching, scaling and erythema of athlete's foot.
  • Seborrheic dermatitis: diminishes scaling, redness and itching on scalp and face.

How It Works

  • Ketoconazole inhibits the fungal enzyme lanosterol 14α‑demethylase, a key step in ergosterol synthesis. By blocking ergosterol production, the drug disrupts the integrity of the fungal cell membrane, leading to impaired growth and eventual cell death of susceptible dermatophytes and yeasts.

Side Effects

Ketoconazole may cause local skin reactions, ranging from mild irritation to rare severe events.

Common Side Effects

  • Burning sensation: mild to moderate discomfort at the application site.
  • Itching: transient pruritus after use.
  • Redness: localized erythema.
  • Dryness: skin may become flaky.
  • Irritation: mild stinging or tingling.
  • Scaling: slight flaking of the treated area.

Serious or Rare Side Effects

  • Allergic reaction: hives, swelling, or difficulty breathing.
  • Severe skin rash: extensive erythema or blistering.
  • Stevens‑Johnson syndrome: rare but life‑threatening mucocutaneous reaction.
  • Liver toxicity: systemic absorption may rarely affect hepatic function.
  • Contact dermatitis: persistent inflammation at the site.
  • Photosensitivity: increased sensitivity to sunlight.

Precautions & Warnings

Before using Ketoconazol Double-E Pharma, consider the following safety measures:

  • Avoid use on broken skin: may increase irritation and systemic absorption.
  • Do not apply to eyes or mucous membranes: can cause significant irritation.
  • Limit exposure to sunlight: may heighten photosensitivity reactions.
  • Discontinue if severe irritation occurs: seek medical advice promptly.
  • Store at room temperature: keep in the original pack, protect from moisture and heat.

Avoid Interactions

Ketoconazol can interact with other medicines, especially those affecting liver enzymes or skin integrity.

Major Interactions (Avoid)

  • Concurrent systemic azole therapy: risk of additive hepatotoxicity.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole oral, itraconazole): may increase systemic levels if absorbed.

Moderate Interactions (Monitor Closely)

  • Topical corticosteroids: may mask irritation signs.
  • Alcohol‑based skin products: can enhance local irritation.
  • Phototoxic agents: increase risk of photosensitivity reactions.

Frequently Asked Questions

Ketoconazol Double-E Pharma is a topical azole antifungal indicated for the treatment of superficial fungal skin infections such as tinea corporis (ringworm), tinea pedis (athlete's foot), and seborrheic dermatitis. It works by eliminating the fungi that cause these conditions, helping to clear lesions, reduce itching and restore normal skin appearance.

Ketoconazole blocks the fungal enzyme lanosterol 14α‑demethylase, which is essential for producing ergosterol, a key component of the fungal cell membrane. Without ergosterol, the membrane becomes defective, leading to impaired growth and death of the fungus. This mechanism targets dermatophytes and yeasts that cause skin infections.

The dosage of Ketoconazol Double-E Pharma is determined by the prescribing healthcare professional based on the specific infection, severity, and patient factors. The product is applied topically to the affected area, typically once or twice daily, as directed by the prescriber. Patients should follow the exact instructions provided on the prescription label.

The safety of topical ketoconazole during pregnancy or lactation has not been definitively established. Healthcare providers usually weigh the potential benefits against any possible risks. Women who are pregnant, planning to become pregnant, or breastfeeding should discuss the use of this product with their doctor before starting treatment.

To order Ketoconazol Double-E Pharma, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide. After receiving the request, the sales team will verify trade or institutional credentials, then provide pricing, availability, shipping details (including any cold‑chain requirements) and necessary import documentation.

Ketoconazol Double-E Pharma belongs to the azole class of antifungals, which inhibit ergosterol synthesis. Compared with allylamine agents such as terbinafine, azoles have a broader spectrum against yeasts but may be associated with higher rates of local irritation. Choice of therapy depends on the specific pathogen, infection site, patient tolerance and prescriber preference.

Ketoconazol Double-E Pharma should be stored at room temperature, below 25 °C. Keep the product in its original packaging, protect it from moisture, direct sunlight and excessive heat. Do not freeze the preparation, and ensure the container is tightly closed when not in use.

The product is applied topically to clean, dry skin in the affected area. A thin layer should be spread evenly, usually once or twice daily as prescribed. Hands should be washed before and after application, and the treated skin should be allowed to dry before covering with clothing or bandages.

Serious risks, though rare, include severe allergic reactions such as anaphylaxis, extensive skin rashes like Stevens‑Johnson syndrome, and systemic toxicity affecting liver function if significant absorption occurs. Patients should stop using the product and seek immediate medical attention if they notice swelling, difficulty breathing, widespread blistering, or signs of liver injury such as jaundice.

Ketoconazol Double-E Pharma should not be used by individuals with known hypersensitivity to ketoconazole or any other azole antifungal. It is also contraindicated on broken, inflamed or infected skin where systemic absorption could be increased, and it should be avoided in the eyes and mucous membranes.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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