EURAX

This brand name is authorized in Canada, France, Hong Kong SAR China, Ireland, Israel, Japan, Mexico, New Zealand, Nigeria, Singapore, Tunisia, UK.

Active ingredients

The drug EURAX contains one active pharmaceutical ingredient (API):

1	Crotamiton UNII D6S4O4XD0H - CROTAMITON
	Crotamiton is a scabicidal and antipruritic agent available as a cream or lotion for topical use only. Crotamiton is usually used to treat pruritis (itching of the skin) caused by scabies or sunburn.
	Read more about Crotamiton

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
EURAX Cream	MPI, EU: SmPC	Medicines & Healthcare Products Regulatory Agency (GB)

Medicine classification

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

ATC Group		Classification
D04AX	Other antipruritics	D Dermatologicals → D04 Antipruritics, incl. antihistamines, anesthetics, etc. → D04A Antipruritics, incl. antihistamines, anesthetics, etc.
Discover more medicines within D04AX
P03AX	Other ectoparasiticides, incl. scabicides	P Antiparasitic products, insecticides and repellents → P03 Ectoparasiticides, incl. scabicides, insecticides and repellents → P03A Ectoparasiticides, incl. scabicides
Discover more medicines within P03AX

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
CA	Health Products and Food Branch	00623377
FR	Base de données publique des médicaments	65623130
GB	Medicines & Healthcare Products Regulatory Agency	26967, 26969
HK	Department of Health Drug Office	00172
IL	מִשְׂרַד הַבְּרִיאוּת	533
JP	医薬品医療機器総合機構	2649722N1027
MX	Comisión Federal para la Protección contra Riesgos Sanitarios	85901
NG	Registered Drug Product Database	04-7299
NZ	Medicines and Medical Devices Safety Authority	1322
SG	Health Sciences Authority	04157P
TN	Direction de la Pharmacie et du Médicament	1623021