Veterinary Medicines

CALMOSYL

Authorised
  • Strychnos ignatii C7
  • Passiflora incarnata C2
  • Zincum metallicum C5
  • MOSCHUS C5
  • Oenanthe crocata C7
  • Datura stramonium C5
  • HYOSCYAMUS NIGER C5
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Product identification

Medicine name:
CALMOSYL
Active substance:
  • Strychnos ignatii C7
  • Passiflora incarnata C2
  • Zincum metallicum C5
  • MOSCHUS C5
  • Oenanthe crocata C7
  • Datura stramonium C5
  • HYOSCYAMUS NIGER C5
Target species:
  • Cattle
  • Pig
  • Horse
  • Horse (mare)
  • Sheep
  • Goat
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Strychnos ignatii C7
    0.14
    gram(s)
    /
    1.00
    millilitre(s)
  • Passiflora incarnata C2
    0.14
    gram(s)
    /
    1.00
    millilitre(s)
  • Zincum metallicum C5
    0.14
    gram(s)
    /
    1.00
    millilitre(s)
  • MOSCHUS C5
    0.14
    gram(s)
    /
    1.00
    millilitre(s)
  • Oenanthe crocata C7
    0.14
    gram(s)
    /
    1.00
    millilitre(s)
  • Datura stramonium C5
    0.14
    gram(s)
    /
    1.00
    millilitre(s)
  • HYOSCYAMUS NIGER C5
    0.14
    gram(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
        day
    • Pig
      • Meat and offal
        0
        day
    • Horse
      • Meat and offal
        0
        day
    • Horse (mare)
      • Milk
        0
        day
    • Sheep
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Goat
      • Meat and offal
        0
        day
      • Milk
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QV03AX
Legal status of supply:
  • Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • France
Available in:
  • France
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Homeopathic medicinal products (Article 19 of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Boiron
Marketing authorisation date:
Manufacturing sites for batch release:
  • Boiron
Responsible authority:
  • French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
  • FR/V/1734122 4/2012
Date of authorisation status change:

Documents

Summary of Product Characteristics

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French (PDF)
Published on: 4/04/2022
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