DIPROSALIC

This brand name is authorized in Austria, Brazil, Canada, Ecuador, Estonia, Finland, France, Hong Kong SAR China, Ireland, Israel, Malta, Netherlands, Poland, Romania, South Africa, Spain, UK.

Active ingredients

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

1
UNII 826Y60901U - BETAMETHASONE DIPROPIONATE
 

Betamethasone is a glucocorticoid which is about eight to ten times as active as prednisolone on a weight-for-weight basis. Betamethasone has anti-inflammatory, antipruritic, and vasoconstrictive properties.

 
Read more about Betamethasone
2
UNII O414PZ4LPZ - SALICYLIC ACID
 

Salicylic acid has bacteriostatic and fungicidal actions, but it is its keratolytic properties which are important for this medicinal product. When applied externally it produces slow and painless destruction of the epithelium.

 
Read more about Salicylic acid

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 DIPROSALIC Ointment 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
D07XC01 Betamethasone D Dermatologicals → D07 Corticosteroids, dermatological preparations → D07X Corticosteroids, other combinations → D07XC Corticosteroids, potent, other combinations
Discover more medicines within D07XC01

Authorization and marketing

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

Country Identification scheme Identifier(s)
BR Câmara de Regulação do Mercado de Medicamentos 540917050029217, 540917050029317, 540917060031117
CA Health Products and Food Branch 00578436
EC Agencia Nacional de Regulación, Control y Vigilancia Sanitaria 367310813
EE Ravimiamet 1006041, 1006074, 1062403, 1062425, 1062436, 1734713, 1865123, 1880805, 1880816
ES Centro de información online de medicamentos de la AEMPS 57463
FI Lääkealan turvallisuus- ja kehittämiskeskus 082040, 418673
FR Base de données publique des médicaments 64435022, 66707065
GB Medicines & Healthcare Products Regulatory Agency 138669, 138671, 143208, 143211, 161591, 161697, 182527, 19266, 19990, 19992
HK Department of Health Drug Office 23072
IE Health Products Regulatory Authority 21474
IL מִשְׂרַד הַבְּרִיאוּת 1244, 1245
MT Medicines Authority AA565/11102, AA565/11105
NL Z-Index G-Standaard 12331600, 12360449
NL Z-Index G-Standaard, PRK 16861
PL Rejestru Produktów Leczniczych 100019516, 100019522, 100257612, 100258534, 100258729, 100265132, 100266077, 100269383, 100326141, 100326566, 100338859, 100345486, 100352760, 100359666, 100413532, 100422778, 100425765, 100440109, 100443770, 100468906
RO Agenția Națională a Medicamentului și a Dispozitivelor Medicale W68209001, W68210001
ZA Health Products Regulatory Authority H/13.4.1/32, L/13.4.1/66

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