Kenocidin 5 mg/ml Teat dip solution
Kenocidin 5 mg/ml Teat dip solution
Authorised
- Chlorhexidine gluconate
Product identification
Medicine name:
Kenocidin, Chlorhexidindigluconat 5 mg/g, Zitzentauchmittel für Rinder (Milchkühe)
Kenocidin 5 mg/ml Teat dip solution
Active substance:
- Chlorhexidine gluconate
Target species:
-
Cattle
Route of administration:
-
Teat use
Product details
Active substance and strength:
-
Chlorhexidine gluconate5.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Teat dip solution
Withdrawal period by route of administration:
-
Teat use
-
Cattle
-
Meat and offalno withdrawal period0 days
-
Milkno withdrawal period0 hours
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QD08AC02
Legal status of supply:
-
Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Austria
Available in:
-
Austria
Package description:
- Kenocidin 5 mg/ml teat dip sol. multidos. cont. 200 l
- Kenocidin 5 mg/ml teat dip sol. multidos. cont. 60 l
- Kenocidin 5 mg/ml teat dip sol. multidos. cont. 25 l
- Kenocidin 5 mg/ml teat dip sol. multidos. cont. 20 l
- Kenocidin 5 mg/ml teat dip sol. multidos. cont. 10 l
- Kenocidin 5 mg/ml teat dip sol. multidos. cont. 5 l
- Kenocidin 5 mg/ml teat dip sol. multidos. cont. 1 l
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 8(3) of Directive No 2001/83/EC)
Marketing authorisation holder:
- Cid Lines
Marketing authorisation date:
Manufacturing sites for batch release:
- Cid Lines
Responsible authority:
- Austrian Agency For Health And Food Safety
Authorisation number:
- 8-00936
Date of authorisation status change:
Reference member state:
-
Belgium
Procedure number:
- BE/V/0039/001
Concerned member states:
-
Austria
-
Bulgaria
-
Cyprus
-
Czechia
-
Estonia
-
France
-
Germany
-
Greece
-
Hungary
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Netherlands
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
English (PDF)
Download Published on: 3/01/2022
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
German (PDF)
Published on: 15/09/2021
Updated on: 15/12/2025
Summary of Product Characteristics
This document does not exist in this language (English). You can find it
in another language below.
German (PDF)
Published on: 6/04/2022
Updated on: 15/12/2025
Labelling
This document does not exist in this language (English). You can find it
in another language below.
German (PDF)
Published on: 15/09/2021
Updated on: 15/12/2025