Veterinary Medicines

Liquid Life Aid Concentrate for Oral Solution for Cattle, Pigs and Sheep

Authorised
  • Glycine
  • Potassium dihydrogen phosphate
  • Sodium propionate
  • Sodium chloride
  • Glucose monohydrate
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Product identification

Medicine name:
Liquid Life Aid Concentrate for Oral Solution for Cattle, Pigs and Sheep
Active substance:
  • Glycine
  • Potassium dihydrogen phosphate
  • Sodium propionate
  • Sodium chloride
  • Glucose monohydrate
Target species:
  • Cattle
  • Sheep
  • Pig
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Glycine
    38.75
    milligram(s)
    /
    1.00
    millilitre(s)
  • Potassium dihydrogen phosphate
    25.43
    milligram(s)
    /
    1.00
    millilitre(s)
  • Sodium propionate
    2.63
    milligram(s)
    /
    1.00
    millilitre(s)
  • Sodium chloride
    53.75
    milligram(s)
    /
    1.00
    millilitre(s)
  • Glucose monohydrate
    306.68
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Oral solution
Withdrawal period by route of administration:
  • Oral use
    • Cattle
      • Meat and offal
        0
        day
      • Milk
        0
        hour
    • Sheep
      • Meat and offal
        0
        day
      • Milk
        0
        hour
    • Pig
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA07CQ02
Legal status of supply:
  • Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Ireland
Package description:
  • The product is marketed in 1 litre translucent high density polyethylene dispenser bottles containing 960 ml. The main chamber of the container is sealed with 38mm diameter tamper proof screw cap and the dispenser chamber is sealed with 28mm diameter tamper proof screw caps

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Complete application (stand-alone) - Council Directive 81/851/EEC
Marketing authorisation holder:
  • Norbrook Laboratories (Ireland) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • Norbrook Laboratories Limited
  • Norbrook Manufacturing Limited
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA22664/023/001
Date of authorisation status change:

Documents

Summary of Product Characteristics

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