Skip to main content
Veterinary Medicines

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/ml Teat dip/spray solution
Active substance:
  • Chlorhexidine gluconate
Target species:
  • Cattle
Route of administration:
  • Teat use

Product details

Active substance and strength:
  • Chlorhexidine gluconate
    5.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Teat dip/spray solution
Withdrawal period by route of administration:
  • Teat use
    • Cattle
      • Meat and offal
        no withdrawal period
      • Milk
        no withdrawal period
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QD08AC02
Authorisation status:
  • Valid
Authorised in:
  • Slovakia
Available in:
  • Slovakia
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
Marketing authorisation holder:
  • Cid Lines
Marketing authorisation date:
Manufacturing sites for batch release:
  • Cid Lines
Responsible authority:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
  • 96/085/MR/15-S
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)

Documents

Combined File of all Documents

This document does not exist in this language (English). You can find it in another language below.
Slovak (PDF)
Published on: 7/03/2023
How useful was this page?:
No votes yet
"Please do not include any personal data, such as your name or contact details. If you do, you consent to the processing of that data in accordance with EMA’s Privacy Statement concerning requests for information or access to documents. If you would like a reply from EMA, please Send a question to EMA instead."