Product image of Hydrocortison-Vaselinecrème Fna Dmb (Hydrocortisone Acetate) supplied by GNH India

Hydrocortison-Vaselinecrème Fna Dmb

Active Ingredient:
Hydrocortisone Acetate
Origin:
EU

Hydrocortison-Vaselinecrème Fna Dmb (Hydrocortisone Acetate)

Hydrocortison-Vaselinecrème Fna Dmb is a topical cream containing the corticosteroid hydrocortisone acetate. It is marketed in the European Union and is formulated for external application to the skin. The product delivers anti‑inflammatory activity through a cream base that facilitates absorption. It is intended for use on inflamed or irritated skin areas under the guidance of a healthcare professional and may be prescribed for various dermatologic conditions.

Manufacturer / TM Owner

Tiofarma B.V.

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Indications & Clinical Uses

Hydrocortison‑Vaselinecrème Fna Dmb is used to manage several inflammatory skin disorders where topical corticosteroid therapy is appropriate.

  • Eczema (atopic dermatitis) affecting mild to moderate areas.
  • Contact dermatitis caused by irritants or allergens.
  • Psoriasis plaques that respond to low‑potency corticosteroids.
  • Seborrheic dermatitis of the scalp or face.
  • Other localized inflammatory skin conditions as determined by a clinician.

How It Works

  • Hydrocortisone acetate penetrates the epidermis and binds to intracellular glucocorticoid receptors. The receptor‑ligand complex translocates to the nucleus, where it interacts with glucocorticoid response elements and modulates transcription of inflammatory genes. This results in decreased synthesis of prostaglandins, cytokines, and other mediators, while also inhibiting leukocyte migration, thereby producing anti‑inflammatory and immunosuppressive effects at the site of application and promotes vasoconstriction, which further reduces edema.

Side Effects

Topical application of hydrocortisone acetate may cause local skin reactions, most of which are mild and reversible.

Common

  • Mild burning or stinging at the application site.
  • Transient itching or redness.
  • Dryness or peeling of the treated skin.
  • Slight skin thinning with prolonged use.

Serious

  • Allergic contact dermatitis manifesting as rash or swelling.
  • Significant skin atrophy or striae.
  • Secondary bacterial, fungal, or viral infection of the area.
  • Systemic absorption leading to adrenal suppression (rare with extensive use).

Precautions & Warnings

Before using Hydrocortison‑Vaselinecrème Fna Dmb, certain safety considerations should be observed to minimize risks.

  • Avoid application to broken, infected, or ulcerated skin unless directed by a physician.
  • Do not use on the face, groin, or axillae for prolonged periods without medical supervision.
  • Limit treatment duration, typically not exceeding two weeks, to reduce the risk of skin atrophy.
  • Discontinue use and seek medical advice if signs of an allergic reaction develop.
  • Use caution in children, pregnant or breastfeeding individuals; consult a healthcare professional first.
  • Keep the product out of reach of children and store at room temperature away from direct sunlight.

Avoid Interactions

Hydrocortison‑Vaselinecrème Fna Dmb can interact with other topical agents or systemic medications that affect corticosteroid activity.

Avoid

  • Concurrent use of other potent topical corticosteroids on the same area.
  • Application of occlusive dressings that increase systemic absorption.

Use with caution

  • Systemic corticosteroids, which may enhance adrenal suppression.
  • Antifungal or antibacterial creams that could irritate the skin when combined.
  • Drugs that affect wound healing, such as retinoids or vitamin A derivatives.
  • Herbal or over‑the‑counter skin products containing irritants.

Frequently Asked Questions

It is indicated for inflammatory skin disorders such as eczema, contact dermatitis, psoriasis plaques, seborrheic dermatitis, and other localized inflammatory conditions as determined by a healthcare professional.

Apply a thin layer to the affected area once or twice daily, gently rubbing it in until the cream is absorbed. Follow the prescribing clinician’s instructions regarding frequency and duration.

Use in children should be under medical supervision, with attention to limited treatment duration and surface area to reduce the risk of systemic absorption and skin thinning.

Common reactions include mild burning, stinging, transient itching, redness, dryness, peeling, and slight skin thinning when used for extended periods.

Typical guidance limits continuous use to about two weeks, unless a healthcare provider advises a longer course based on the specific condition and response.

Facial use should be limited and only under medical advice, as the skin on the face is more sensitive and prone to thinning and irritation.

Discontinue the product immediately and seek medical evaluation. An allergic reaction may present as rash, swelling, or severe itching.

Concurrent use may be possible, but it should be coordinated by a healthcare professional to avoid skin irritation or reduced efficacy.

Systemic absorption is generally low but can occur with extensive application, occlusion, or prolonged use, potentially affecting adrenal function.

Store at room temperature, away from direct sunlight and moisture. Keep the container tightly closed and out of reach of children.

Pregnancy and breastfeeding status should be discussed with a healthcare provider before use, as safety data for topical hydrocortisone acetate are limited.

It combines hydrocortisone acetate with a Vaseline-based cream vehicle, which may enhance skin moisturization and drug absorption compared with some other formulations.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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