Veterinary Medicines

Alcide UDDERgold Platinum

Authorised
  • Lactic acid
  • Sodium chlorite
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Product identification

Medicine name:
Alcide UDDERgold Platinum
Alcide UDDERgold Platinum
Active substance:
  • Lactic acid
  • Sodium chlorite
Target species:
  • Cattle
Route of administration:
  • Teat 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:
  • Teat 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:
  • Valid
Authorised in:
  • Ireland
Package description:
  • Base and Activator are supplied separately, packed in pairs of high density polyethylene (HDPE) bottles/container withpolypropylene 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 withpolypropylene 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 withpolypropylene 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:
  • Ferdinand Eimermacher GmbH und Co. KG
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA10795/003/001
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0572/001
Concerned member states:
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

English (PDF)
Published on: 3/05/2024
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