File downloaded on 2026-04-05
Source URL: https://medicines.health.europa.eu/veterinary/en/600000006070
Authorised

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
        0
        day
      • Milk
        0
        hour
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QD08AC02
Legal status of supply:
  • Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Slovenia
Available in:
  • Slovenia
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:
  • Agency For Medicinal Products And Medical Devices Of The Republic Of Slovenia
Authorisation number:
  • MR/V/0378/001
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

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 2/02/2022
Download

Package Leaflet and Labelling

This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 2/02/2022
Download