Veterinary Medicines

OSTEOTRAUMYL POUDRE ORALE

Authorised
  • CALCIUM CARBONICUM HAHNEMANNI D3
  • RUTA GRAVEOLENS D3
  • SYMPHYTUM OFFICINALE D3
  • ARNICA MONTANA D3
  • SULFUR IODATUM D3
  • CALCAREA PHOSPHORICA D3
  • CALCIUM FLUORATUM D3
Download as PDF

Product identification

Medicine name:
OSTEOTRAUMYL POUDRE ORALE
Active substance:
  • CALCIUM CARBONICUM HAHNEMANNI D3
  • RUTA GRAVEOLENS D3
  • SYMPHYTUM OFFICINALE D3
  • ARNICA MONTANA D3
  • SULFUR IODATUM D3
  • CALCAREA PHOSPHORICA D3
  • CALCIUM FLUORATUM D3
Target species:
  • Cattle
  • Pig
  • Equid
  • Sheep
  • Goat
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • CALCIUM CARBONICUM HAHNEMANNI D3
    0.14
    gram(s)
    /
    1.00
    gram(s)
  • RUTA GRAVEOLENS D3
    0.14
    gram(s)
    /
    1.00
    gram(s)
  • SYMPHYTUM OFFICINALE D3
    0.14
    gram(s)
    /
    1.00
    gram(s)
  • ARNICA MONTANA D3
    0.14
    gram(s)
    /
    1.00
    gram(s)
  • SULFUR IODATUM D3
    0.10
    gram(s)
    /
    1.00
    gram(s)
  • CALCAREA PHOSPHORICA D3
    0.14
    gram(s)
    /
    1.00
    gram(s)
  • CALCIUM FLUORATUM D3
    0.10
    gram(s)
    /
    1.00
    gram(s)
Pharmaceutical form:
  • Oral powder
Withdrawal period by route of administration:
  • Oral use
    • Cattle
      • Meat and offal
        0
        day
      • Milk
        no withdrawal period
    • Pig
      • Meat and offal
        0
        day
    • Equid
      • Meat and offal
        0
        day
      • Milk
        no withdrawal period
    • Sheep
      • Meat and offal
        0
        day
      • Milk
        no withdrawal period
    • Goat
      • Meat and offal
        0
        day
      • Milk
        no withdrawal period
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
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/0913144 6/2012
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: 3/11/2025
Download

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: 3/11/2025
Download