OCTENISEPT

1MG/G+20MG/G DRM SOL 1X500ML

SÚKL code 0023988
Name of the product OCTENISEPT
_MA_MEDICATION_DETAIL_INFO_MED_NAME i OCTENISEPT
Supplement 1MG/G+20MG/G DRM SOL 1X500ML
Strenght 1MG/G+20MG/G
Pharmaceutical form Cutaneous solution
Package 1X500ML
Route Cutaneous use
Language of the pack Czech
Wrap type Bottle
Legal status OTC medicinal products
Active substance PHENOXYETHANOL (PHENOXYETHANOLUM)
OCTENIDINE DIHYDROCHLORIDE (OCTENIDINI DIHYDROCHLORIDUM)
ATC group D08AJ57
ATC group name OKTENIDIN, KOMBINACE

Marketing authorisation information

Registration Number 32/ 558/08-C
Type of MA National
MA status B - medicinal product after change, may be placed on the market for the period of 6 months (Placed on the market till) and used until expiration, not later than till the end of validity of the marketing authorisation (Valid till)
Placed on the market till 30. 09. 2016
MA Holder Schülke & Mayr GmbH, Vídeň
MA Holder country RAKOUSKO
Actual MA holder Schülke & Mayr GmbH, Norderstedt
Actual MA holder country NĚMECKO

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