OCTENISEPT

This brand name is authorized in Austria, Estonia, Croatia, Malta, New Zealand, Poland, Romania, Turkey

Active ingredients

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

1 Octenidine UNII U84956NU4B - OCTENIDINE HYDROCHLORIDE

Read about Octenidine

2 Phenoxyethanol UNII HIE492ZZ3T - PHENOXYETHANOL

Read about Phenoxyethanol

Medicine classification

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

ATC code	Group title	Classification
D08AJ57	Octenidine, combinations	D Dermatologicals → D08 Antiseptics and disinfectants → D08A Antiseptics and disinfectants → D08AJ Quaternary ammonium compounds
Discover more medicines within D08AJ57

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
Country: EE	Ravimiamet	Identifier(s): 1637782, 1637793, 1637805, 1637816, 1655849, 1655850, 1660171
Country: HR	Agencija za lijekove i medicinske proizvode	Identifier(s): HR-H-068837892
Country: MT	Medicines Authority	Identifier(s): AA1247/00201
Country: NZ	Medicines and Medical Devices Safety Authority	Identifier(s): 19633
Country: PL	Rejestru Produktów Leczniczych	Identifier(s): 100048742, 100283450, 100291572, 100303565, 100306084, 100307043, 100331366, 100351742, 100361887, 100403812, 100424369, 100443154
Country: RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	Identifier(s): W01962003, W01962004, W01962005
Country: TR	İlaç ve Tıbbi Cihaz Kurumu	Identifier(s): 8697621750166, 8699473650014, 8699473650021, 8699473650038, 8699473650045