Veterinary Medicines

Uierbalsem, emulsie voor uitwendig gebruik

Authorised
  • LAUREL LEAF OIL
  • ROSEMARY OIL
  • CLOVE OIL
  • ARNICA TINCTURE
  • EUCALYPTUS OIL
  • Camphor, racemic
  • HYPERICI OLEUM
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Product identification

Medicine name:
Uierbalsem, emulsie voor uitwendig gebruik
Active substance:
  • LAUREL LEAF OIL
  • ROSEMARY OIL
  • CLOVE OIL
  • ARNICA TINCTURE
  • EUCALYPTUS OIL
  • Camphor, racemic
  • HYPERICI OLEUM
Target species:
  • Cattle
  • Ruminant
  • Goat (adult female)
  • Sheep
  • Equid
Route of administration:
  • Teat use

Product details

Active substance and strength:
  • LAUREL LEAF OIL
    5.00
    milligram(s)
    /
    1.00
    gram(s)
  • ROSEMARY OIL
    5.00
    milligram(s)
    /
    1.00
    gram(s)
  • CLOVE OIL
    0.60
    milligram(s)
    /
    1.00
    gram(s)
  • ARNICA TINCTURE
    25.00
    milligram(s)
    /
    1.00
    gram(s)
  • EUCALYPTUS OIL
    20.00
    milligram(s)
    /
    1.00
    gram(s)
  • Camphor, racemic
    25.00
    milligram(s)
    /
    1.00
    gram(s)
  • HYPERICI OLEUM
    100.00
    milligram(s)
    /
    1.00
    gram(s)
Pharmaceutical form:
  • Cutaneous emulsion
Withdrawal period by route of administration:
  • Teat use
    • Cattle
      • Milk
        no withdrawal period
      • Meat and offal
        no withdrawal period
    • Ruminant
      • Milk
        no withdrawal period
      • Meat and offal
        no withdrawal period
    • Goat (adult female)
      • Milk
        no withdrawal period
      • Meat and offal
        no withdrawal period
    • Sheep
      • Milk
        no withdrawal period
      • Meat and offal
        no withdrawal period
    • Equid
      • Meat and offal
        no withdrawal period
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QG52C
Legal status of supply:
  • Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Netherlands
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
  • SaluVet GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • SaluVet GmbH
Responsible authority:
  • Medicines Evaluation Board
Authorisation number:
  • REG NL 5627
Date of authorisation status change:

Documents

Combined File of all Documents

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Dutch (PDF)
Published on: 24/02/2022
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