EURAX

This brand name is authorized in Canada, France, Hong Kong, Ireland, Israel, Japan, Mexico, Nigeria, New Zealand, Singapore, Tunisia, United Kingdom

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 about Crotamiton

Medication package inserts

Below package inserts are available for further reading:

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

Medicine classification

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

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

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