PHYTOLAC SOLUTION BUVABLE
PHYTOLAC SOLUTION BUVABLE
Authorised
- Atropa bella-donna C5
- HEPAR SULFURIS C7
- PYROGENIUM C7
- Phytolacca americana C5
- Conium maculatum C5
- STREPTOCOCCINUM C5
- STAPHYLOCOCCINUM C5
- Pulsatilla vulgaris C5
- APIS MELLIFICA C5
Product identification
Medicine name:
PHYTOLAC SOLUTION BUVABLE
Active substance:
- Atropa bella-donna C5
- HEPAR SULFURIS C7
- PYROGENIUM C7
- Phytolacca americana C5
- Conium maculatum C5
- STREPTOCOCCINUM C5
- STAPHYLOCOCCINUM C5
- Pulsatilla vulgaris C5
- APIS MELLIFICA C5
Target species:
-
Cattle (cow)
-
Sheep (ewe)
-
Goat (adult female)
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Atropa bella-donna C5108.80/milligram(s)1.00millilitre(s)
-
HEPAR SULFURIS C7108.80/milligram(s)1.00millilitre(s)
-
PYROGENIUM C7108.80/milligram(s)1.00millilitre(s)
-
Phytolacca americana C5108.80/milligram(s)1.00millilitre(s)
-
Conium maculatum C5108.80/milligram(s)1.00millilitre(s)
-
STREPTOCOCCINUM C5108.80/milligram(s)1.00millilitre(s)
-
STAPHYLOCOCCINUM C5108.80/milligram(s)1.00millilitre(s)
-
Pulsatilla vulgaris C5108.80/milligram(s)1.00millilitre(s)
-
APIS MELLIFICA C5108.80/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Oral solution
Withdrawal period by route of administration:
-
Oral use
-
Cattle (cow)
-
Meat and offal0day
-
Milk0dayNe pas livrer le lait du ou des quartiers traités pendant la durée du traitement.
-
-
Sheep (ewe)
-
Meat and offal0day
-
Milkno withdrawal periodNe pas livrer le lait du ou des quartiers traités pendant la durée du traitement.
-
-
Goat (adult female)
-
Meat and offal0day
-
Milkno withdrawal periodNe pas livrer le lait du ou des quartiers traités pendant la durée du traitement.
-
-
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
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/6233547 2/2007
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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: 13/10/2025
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: 13/10/2025