IBUGEL

5 %w/w Gel

Dermal Laboratories LtdPA0278/020/001

Main Information

Trade NameIBUGEL
Active SubstancesIBUPROFEN
Strength5 %w/w
Dosage FormGel
Licence HolderDermal Laboratories Ltd
Licence NumberPA0278/020/001

Group Information

ATC CodeM02AA13 Antiinflammatory preparations, non-steroids for topical use

Status

Authorised/WithdrawnAuthorised
Licence Issued19/09/1995
Supply StatusSupply through pharmacies only
Dispensing StatusProduct subject to prescription which may be renewed (B)
Marketing StatusMarketed
Promotion StatusPromotion to Healthcare Professionals only
Conditions of Licence

Documents

Summary of Product CharacteristicsPDF Version
Package LeafletPDF Version
Public Assessment ReportNo document available
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Latest Changes to Medicine Info & SPC

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Please note changes to the medicine information and summary of product characteristics are only available from the 19/05/2015 onwards. Changes made before this date aren't available online.