Alcide UDDERgold Platinum
Alcide UDDERgold Platinum
Not authorised
- Sodium chlorite
- Lactic acid
Product identification
Medicine name:
Alcide UDDERgold Platinum
Alcide Uddergold PM Vet 26.4 mg/ml Concentraat voor dipoplossing
Alcide Uddergold PM Vet 26.4 mg/ml Solution à diluer pour trempage
Alcide Uddergold PM Vet 26.4 mg/ml Konzentrat zur Herstellung eines Tauchbades, Lösung
Active substance:
- Sodium chlorite
- Lactic acid
Target species:
-
Cattle
Route of administration:
-
Topical use
Product details
Active substance and strength:
-
Sodium chlorite6.40milligram(s)1.00millilitre(s)
-
Lactic acid26.40milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Concentrate for dip solution
Withdrawal period by route of administration:
-
Topical use
- Cattle
-
Meat and offal0day
-
Milk0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QG52A
Legal status of supply:
-
Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Belgium
Package description:
- Base and Activator are supplied separately, packed in pairs of high density polyethylene (HDPE) bottles/containers with polypropylene or HDPE screw caps holding 3.785 litres of the Base or Activator component.
- Base and Activator are supplied separately, packed in pairs of high density polyethylene (HDPE) bottles/container with polypropylene or HDPE screw caps holding 20 litres of the Base or Activator component.
- Base and Activator are supplied separately, packed in pairs of high density polyethylene (HDPE) bottles/containers with polypropylene or HDPE screw caps holding 10 litres of the Base or Activator component.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Ecolab Deutschland GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Ecolab Deutschland GmbH
Responsible authority:
- FAMHP
Authorisation number:
- BE-V318631
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0572/001
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
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