TRAVOCORT

This brand name is authorized in Austria, Croatia, Cyprus, Estonia, Hong Kong SAR China, Ireland, Lithuania, Malta, Poland, Romania, Singapore, South Africa, Turkey.

Active ingredients

The drug TRAVOCORT contains a combination of these active pharmaceutical ingredients (APIs):

1	Isoconazole UNII 5AS8P3N30X - ISOCONAZOLE NITRATE
	Isoconazole is for use in the treatment of superficial fungal diseases of the skin. It displays a very broad spectrum of antimicrobial action. It is effective against dermatophytes and yeasts, yeast-like fungi (including the causative organism of pityriasis versicolor) and molds, as well against gram-positive bacteria in-vitro and against the causative organism of erythrasma.
	Read more about Isoconazole
2	Diflucortolone UNII 1A63Z067C8 - DIFLUCORTOLONE VALERATE
	Diflucortolone is a topically acting fluoridated corticosteroid which suppresses inflammation in inflammatory and allergic skin conditions and alleviates the subjective complaints such as itching, burning and pain.
	Read more about Diflucortolone

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
TRAVOCORT Cream	MPI, EU: SmPC	Health Products Regulatory Authority (IE)

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group		Classification
D01AC20	Combinations	D Dermatologicals → D01 Antifungals for dermatological use → D01A Antifungals for topical use → D01AC Imidazole and triazole derivatives
Discover more medicines within D01AC20

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country	Identification scheme	Identifier(s)
EE	Ravimiamet	1000416, 1061008, 1783830, 1827659
HK	Department of Health Drug Office	43659
HR	Agencija za lijekove i medicinske proizvode	HR-H-939866694
IE	Health Products Regulatory Authority	78751
LT	Valstybinė vaistų kontrolės tarnyba	1007947, 1072785, 1080556, 1085844, 1089160, 1090097, 1093551
MT	Medicines Authority	MA024/01901, PI908/03701A
PL	Rejestru Produktów Leczniczych	100067640, 100075740, 100257552, 100268573, 100286849, 100291690, 100323898, 100324640, 100326537, 100327117, 100345523, 100346899, 100394817, 100395521, 100422034, 100456750, 100460400
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W66599001
SG	Health Sciences Authority	04564P
TR	İlaç ve Tıbbi Cihaz Kurumu	8699514350194
ZA	Health Products Regulatory Authority	N/13.4.1/171