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HSA Approval

TRAVOCORT CREAM

SIN04564P

TRAVOCORT CREAM

TRAVOCORT CREAM

May 31, 1990

DKSH SINGAPORE PTE. LTD.

DKSH SINGAPORE PTE. LTD.

Regulatory Information

DKSH SINGAPORE PTE. LTD.

DKSH SINGAPORE PTE. LTD.

Therapeutic

Prescription Only

Formulation Information

CREAM

**Dosage and administration** Cutaneous use. Travocort should be applied twice daily to the diseased areas of skin. The treatment with Travocort must be terminated after regression of the inflammatory or eczematous skin condition, at the latest, however, after 2 weeks, and the therapy continued or followed up with a glucocorticoid-free anti-fungal preparation. This applies in particular for use in the inguinal and genital regions.

TOPICAL

Medical Information

**Indications** Initial or interim treatment of those superficial fungal infections of the skin which are accompanied by highly inflammatory or eczematous skin conditions, e.g. in the region of the hands, the interdigital spaces of the feet, and the inguinal and genital regions.

**Contraindications** Tuberculous or syphilitic processes in the area to be treated; virus diseases (e.g. varicella, herpes zoster), rosacea, perioral dermatitis and postvaccination skin reactions in the area to be treated.

D01AC20

imidazoles/triazoles in combination with corticosteroids

Manufacturer Information

DKSH SINGAPORE PTE. LTD.

LEO Pharma Manufacturing Italy S.r.I

Active Ingredients

ISOCONAZOLE NITRATE

10 mg/g

Isoconazole

DIFLUCORTOLONE VALERATE

1 mg/g

Difluocortolone

Documents

Package Inserts

063581_3.pdf

Approved: September 27, 2019

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