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National Drug Formulary

ELOMET OINTMENT 0.1% [SIN07566P]

Active ingredients: ELOMET OINTMENT 0.1%

View product's general information
Last updated 24 April 2026

Product Info

ELOMET OINTMENT 0.1%

[SIN07566P]

Product information

Active Ingredient and Strength

MOMETASONE FUROATE ANHYDROUS - 0.1%

Dosage Form

OINTMENT

Manufacturer and Country

PT ORGANON PHARMA INDONESIA TBK - INDONESIA REP OF

Registration Number

SIN07566P

Licence Holder

ORGANON SINGAPORE PTE. LTD.

Forensic Classification

PRESCRIPTION ONLY MEDICINES

Anatomical Therapeutic Chemical (ATC) code

D07AC13

Prescription-only Medicines with Exemptions for Supply without Prescription

As a topical preparation as a single agent not exceeding 0.1%

  • Indications: Symptomatic relief of inflammatory skin or scalp disorders such as dermatitis and eczema.

  • Maximum daily dose: Apply to the affected areas once daily

  • Maximum supply: 15g for cream/ointment/gel

  • 30ml for topical solution

  • Minimum age: 18 years

Indication

INDICATIONS AND USAGE:
ELOMET Ointment 0.1% is indicated for the relief of the inflammatory and pruritic manifestations of corticosteroid responsive dermatoses. The lotion formulation may be applied to scalp lesions.

Dosing

DOSAGE AND ADMINISTRATION:
A thin film of ELOMET Ointment 0.1% should be applied to the affected skin areas once daily until the lesion heals or for a duration of three weeks, whichever is sooner.

Contraindications

CONTRAINDICATIONS:
ELOMET Ointment 0.1% is contraindicated in patients who are sensitive to mometasone furoate, to other corticosteroids or to any component of these preparations.