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FML LIQUIFILM OPHTHALMIC SUSPENSION 0.1% [SIN04347P]

Active ingredients: FML LIQUIFILM OPHTHALMIC SUSPENSION 0.1%

Last updated 26 October 2025

Product Info

FML LIQUIFILM OPHTHALMIC SUSPENSION 0.1%

[SIN04347P]

Product information

Active Ingredient and Strength

FLUOROMETHOLONE - 0.1% W/V

Dosage Form

SOLUTION

Manufacturer and Country

ALLERGAN PHARMACEUTICALS IRELAND - IRELAND

Registration Number

SIN04347P

Licence Holder

ABBVIE PTE. LTD.

Forensic Classification

PRESCRIPTION ONLY MEDICINES

Anatomical Therapeutic Chemical (ATC) code

S01BA07

INDICATIONS
For steroid responsive inflammation of the palpebral and bulbar conjunctiva, cornea and anterior segment of the globe.

DOSAGE AND ADMINISTRATION
1 to 2 drops instilled into the conjunctival sac two to four times daily. During the initial 24 to 48 hours the dosage may be safely increased to 2 drops every hour. Care should be taken not to discontinue therapy prematurely.

The dosing of fluorometholone ophthalmic suspension 0.1% may be reduced, but care should be taken not to discontinue therapy prematurely. In chronic conditions, withdrawal of treatment should be carried out by gradually decreasing the frequency of applications.

CONTRAINDICATIONS
Acute superficial (or epithelial) herpes simplex keratitis (dendritic keratitis).
Fungal diseases of ocular structures.
Vaccinia, varicella and most other viral diseases of the cornea and conjunctiva.
Mycobacterial infection such as tuberculosis of the eye. Hypersensitivity to the constituents of this medication.