Veterinary Medicines

CERVICYL SOLUTION BUVABLE

Authorised
  • CIMICIFUGA RACEMOSA C5
  • Secale cornutum C5
  • GELSEMIUM SEMPERVIRENS C5
  • Caulophyllum thalictroides C5
  • Atropa bella-donna C5
  • ARNICA MONTANA C5
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Product identification

Medicine name:
CERVICYL SOLUTION BUVABLE
Active substance:
  • CIMICIFUGA RACEMOSA C5
  • Secale cornutum C5
  • GELSEMIUM SEMPERVIRENS C5
  • Caulophyllum thalictroides C5
  • Atropa bella-donna C5
  • ARNICA MONTANA C5
Target species:
  • Cattle (cow)
  • Pig (sow)
  • Horse (mare)
  • Sheep (ewe)
  • Goat (adult female)
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • CIMICIFUGA RACEMOSA C5
    163.20
    milligram(s)
    /
    1.00
    millilitre(s)
  • Secale cornutum C5
    163.20
    milligram(s)
    /
    1.00
    millilitre(s)
  • GELSEMIUM SEMPERVIRENS C5
    163.20
    milligram(s)
    /
    1.00
    millilitre(s)
  • Caulophyllum thalictroides C5
    163.20
    milligram(s)
    /
    1.00
    millilitre(s)
  • Atropa bella-donna C5
    163.20
    milligram(s)
    /
    1.00
    millilitre(s)
  • ARNICA MONTANA C5
    163.20
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Oral solution
Withdrawal period by route of administration:
  • Oral use
    • Cattle (cow)
      • All relevant tissues
        0
        day
    • Pig (sow)
      • All relevant tissues
        0
        day
    • Horse (mare)
      • All relevant tissues
        0
        day
    • Sheep (ewe)
      • All relevant tissues
        0
        day
    • Goat (adult female)
      • All relevant tissues
        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/9599938 4/2012
Date of authorisation status change:

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 1/08/2025
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Package Leaflet and Labelling

This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 1/08/2025
Download