NERISONE

This brand name is authorized in Germany, France, Hong Kong, New Zealand, United Kingdom, South Africa

Active ingredients

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

1 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 about Diflucortolone

Medication package inserts

Below package inserts are available for further reading:

Title Information Source Document Type  
NERISONE Cream, Ointment Medicines and Medical Devices Safety Authority (NZ) 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
D07AC06 Diflucortolone D Dermatologicals → D07 Corticosteroids, dermatological preparations → D07A Corticosteroids, plain → D07AC Corticosteroids, potent (group III)
Discover more medicines within D07AC06

Authorization and marketing

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

Country Identification scheme Identifier(s)
Country: DE Bundesinstitut fรผr Arzneimittel und Medizinprodukte Identifier(s): 00247315, 00247338, 00247545, 00247893, 07548273, 07548296
Country: FR Base de donnรฉes publique des mรฉdicaments Identifier(s): 62017113, 63420875, 67945482
Country: GB Medicines & Healthcare Products Regulatory Agency Identifier(s): 25698, 38360, 38367, 39616, 39623
Country: HK Department of Health Drug Office Identifier(s): 43570
Country: NZ Medicines and Medical Devices Safety Authority Identifier(s): 2372
Country: ZA Health Products Regulatory Authority Identifier(s): H/13.4.1/218, H/13.4.1/219, H/13.4.1/220, R/13.4.1/26, R/13.4.1/27

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