Veterinary Medicines

Alcide UDDERgold Platinum

Not authorised
  • Lactic acid
  • Sodium chlorite
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Product identification

Medicine name:
Alcide UDDERgold Platinum
Alcide UDDERgold PM vet, concentraten (Base en Activator) voor tepeldipoplossing voor rundvee (melkvee)
Active substance:
  • Lactic acid
  • Sodium chlorite
Target species:
  • Cattle
Route of administration:
  • Topical use

Product details

Active substance and strength:
  • Lactic acid
    26.40
    milligram(s)
    /
    1.00
    millilitre(s)
  • Sodium chlorite
    6.40
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Concentrate for dip solution
Withdrawal period by route of administration:
  • Topical use
    • Cattle
      • Meat and offal
        0
        day
      • Milk
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QG52A
Legal status of supply:
  • Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
  • Surrendered
Authorised in:
  • Netherlands
Package description:
  • 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.
  • 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.

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:
  • MEB
Authorisation number:
  • REG NL 101795
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0572/001

Documents

Summary of Product Characteristics

English (PDF)
Published on: 8/04/2022
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Combined File of all Documents

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 30/06/2022
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