Product image of Mofur (Mometasone Furoate) supplied by GNH India

Mofur

Active Ingredient:
Mometasone Furoate
Origin:
EU

Mofur (Mometasone Furoate)

Mometasone Furoate, the active ingredient in Mofur, is a corticosteroid (glucocorticoid) presented as a topical formulation for skin use. It is prescribed to reduce inflammation and itching associated with various dermatologic conditions in patients of all ages.

GNH India supplies Mofur as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides regulatory‑approved batches to meet global demand. Customers benefit from reliable logistics and dedicated technical support.

Manufacturer / TM Owner

Gabriel Health

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Indications & Clinical Uses

  • Mometasone Furoate is used topically to manage inflammatory skin disorders.
  • Eczema: alleviates redness, swelling, and itching, helping restore skin barrier function in affected areas.
  • Psoriasis: reduces plaque formation and scaling, providing symptomatic relief in chronic plaque psoriasis.
  • Atopic dermatitis: diminishes flare‑ups by suppressing immune‑mediated inflammation and pruritus.
  • Contact dermatitis: mitigates acute inflammatory response caused by irritants or allergens, decreasing erythema and discomfort.

How It Works

  • Mometasone Furoate binds to intracellular glucocorticoid receptors in keratinocytes and immune cells. The receptor complex translocates to the nucleus, where it interacts with glucocorticoid response elements, modulating transcription of anti‑inflammatory proteins and repressing pro‑inflammatory cytokines such as IL‑1, IL‑6, and TNF‑α. This results in reduced cellular infiltration, edema, and immune activation in the skin.

Side Effects

Topical application of Mometasone Furoate may be associated with local and, rarely, systemic adverse reactions.

Common Side Effects

  • Skin irritation or burning sensation
  • Pruritus or itching at application site
  • Dryness or flaking of the skin
  • Acne or folliculitis development

Serious or Rare Side Effects

  • Skin atrophy or thinning with prolonged use
  • Hypothalamic‑pituitary‑adrenal axis suppression
  • Severe allergic reactions such as angioedema or anaphylaxis

Precautions & Warnings

  • When prescribing or using Mometasone Furoate, several precautions should be observed to minimize risk.
  • Apply to affected area only: limit use to diagnosed skin lesions.
  • Avoid use on broken or infected skin: may increase systemic absorption.
  • Do not use with occlusive dressings: can enhance drug penetration and side effects.
  • Limit duration of therapy: follow physician guidance to prevent skin atrophy.
  • Store at room temperature: keep in original container, protect from moisture and light.

Avoid Interactions

Mometasone Furoate can interact with other medications, affecting its safety or efficacy.

Major Interactions (Avoid)

  • Systemic corticosteroids: additive systemic glucocorticoid effects may cause adrenal suppression.
  • Potent CYP3A4 inhibitors (e.g., ketoconazole): may increase local drug levels and risk of side effects.
  • Live vaccines: topical steroid may reduce local immune response, potentially compromising vaccine efficacy.

Moderate Interactions (Monitor Closely)

  • Topical antibiotics (e.g., mupirocin): increased risk of skin irritation.
  • Phototherapy (UVB): may enhance photosensitivity and skin damage.
  • Other topical steroids: cumulative potency may raise risk of skin atrophy.

Frequently Asked Questions

Mofur, containing Mometasone Furoate, is prescribed for inflammatory skin disorders such as eczema, psoriasis, atopic dermatitis, and contact dermatitis. It helps reduce redness, swelling, and itching associated with these conditions when applied to the affected skin areas.

Mometasone Furoate binds to glucocorticoid receptors inside skin cells, altering gene transcription. This suppresses pro‑inflammatory cytokines and promotes anti‑inflammatory proteins, leading to decreased cellular infiltration, edema, and immune activity in the skin.

The prescribed dose of Mofur is determined by the treating clinician based on the severity of the skin condition, the area to be treated, patient age, and any previous response to therapy. No universal dosing regimen is provided.

Safety data for Mometasone Furoate in pregnancy and lactation are limited. The product should only be used if the potential benefit justifies any potential risk to the fetus or infant, and this decision must be made by a qualified health professional.

To order Mofur, submit an enquiry on the product page at gnhindia.com with 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.

Mofur (Mometasone Furoate) and betamethasone are both potent topical glucocorticoids, but they differ in potency, formulation options and specific regulatory approvals. Clinical choice depends on the condition being treated, physician preference, and patient tolerance to each agent.

Store Mofur at room temperature, preferably below 25 °C. Keep the product in its original packaging, protect it from moisture, excessive heat and direct sunlight to maintain stability and potency.

Apply a thin layer of Mofur to the clean, dry affected skin area once or twice daily as directed by the prescriber. Gently rub the medication until it disappears, and wash hands after application unless the hands are being treated.

Serious risks include skin atrophy (thinning), hypothalamic‑pituitary‑adrenal axis suppression with extensive use, and severe allergic reactions such as angioedema or anaphylaxis. Patients should report any unusual skin changes, systemic symptoms or signs of infection promptly.

Mofur should be avoided in individuals with known hypersensitivity to Mometasone Furoate or any excipients, in patients with untreated fungal, bacterial, viral or tuberculous skin infections, and in those where systemic corticosteroid therapy is contraindicated unless specifically advised by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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