Kenocidin Spray and Dip Chloorhexidine Digluconaat 5 mg/ml Teat dip/spray solution
Kenocidin Spray and Dip Chloorhexidine Digluconaat 5 mg/ml Teat dip/spray solution
Authorised
- Chlorhexidine gluconate
Product identification
Medicine name:
Kenocidin Spray and Dip Chloorhexidine Digluconaat 5 mg/g Tepeldip/tepelspray, oplossing
Kenocidin Spray and Dip Chloorhexidine Digluconaat 5 mg/g Solution pour trempage/pulvérisation mammaire
Kenocidin Spray and Dip Chloorhexidine Digluconaat 5 mg/g Zitzentauchmittel/Zitzenspray Lösung
Kenocidin Spray and Dip Chloorhexidine Digluconaat 5 mg/ml Teat dip/spray solution
Active substance:
- Chlorhexidine gluconate
Target species:
-
Cattle
Route of administration:
-
Teat use
Product details
Active substance and strength:
-
Chlorhexidine gluconate5.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Teat dip/spray 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:
-
Belgium
Available in:
-
Belgium
Package description:
- Kenocidin Spray and Dip Chloorhexidine Digluconaat 5 mg/ml teat dip/teat spray sol. multidos. cont. 200 l
- Kenocidin Spray and Dip Chloorhexidine Digluconaat 5 mg/ml teat dip/teat spray sol. multidos. cont. 60 l
- Kenocidin Spray and Dip Chloorhexidine Digluconaat 5 mg/ml teat dip/teat spray sol. multidos. cont. 25 l
- Kenocidin Spray and Dip Chloorhexidine Digluconaat 5 mg/ml teat dip/teat spray sol. multidos. cont. 20 l
- Kenocidin Spray and Dip Chloorhexidine Digluconaat 5 mg/ml teat dip/teat spray sol. multidos. cont. 10 l
- Kenocidin Spray and Dip Chloorhexidine Digluconaat 5 mg/ml teat dip/teat spray sol. multidos. cont. 5 l
- Kenocidin Spray and Dip Chloorhexidine Digluconaat 5 mg/ml teat dip/teat spray 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:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V393592
Date of authorisation status change:
Reference member state:
-
Belgium
Procedure number:
- BE/V/0040/001
Concerned member states:
-
Bulgaria
-
Cyprus
-
Czechia
-
Estonia
-
France
-
Germany
-
Greece
-
Hungary
-
Ireland
-
Latvia
-
Lithuania
-
Luxembourg
-
Malta
-
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: 4/01/2022
Package Leaflet
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Summary of Product Characteristics
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