Rhus/Aconitum comp. PlantaVet Flüssige Verdünnung zur Injektion für Pferde, Rinder, Schweine, Schafe, Ziegen
Rhus/Aconitum comp. PlantaVet Flüssige Verdünnung zur Injektion für Pferde, Rinder, Schweine, Schafe, Ziegen
Authorised
- RHUS TOXICODENDRON D5
- MANDRAGORA OFFICINARUM E RADICE FERM 34D DIL. D5 (HAB, VS. 34D)
- LEONTOPODIUM ALPINUM E PLANTA TOTA FERM 36 DIL. D3 (HAB, VS. 36)
- GRANIT DIL. D9 (HAB, VS. 6)
- GELSEMIUM SEMPERVIRENS E RHIZOMA FERM 35B DIL. D3 (HAB, VS. 35B)
- ACONITUM NAPELLUS E TUBERE FERM 33C DIL. D5 (HAB, VS. 33C)
Product identification
Medicine name:
Rhus/Aconitum comp. PlantaVet Flüssige Verdünnung zur Injektion für Pferde, Rinder, Schweine, Schafe, Ziegen
Active substance:
- RHUS TOXICODENDRON D5
- MANDRAGORA OFFICINARUM E RADICE FERM 34D DIL. D5 (HAB, VS. 34D)
- LEONTOPODIUM ALPINUM E PLANTA TOTA FERM 36 DIL. D3 (HAB, VS. 36)
- GRANIT DIL. D9 (HAB, VS. 6)
- GELSEMIUM SEMPERVIRENS E RHIZOMA FERM 35B DIL. D3 (HAB, VS. 35B)
- ACONITUM NAPELLUS E TUBERE FERM 33C DIL. D5 (HAB, VS. 33C)
Target species:
-
Cattle
-
Goat
-
Sheep
-
Horse
-
Pig
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
RHUS TOXICODENDRON D51.00gram(s)10.00millilitre(s)
-
MANDRAGORA OFFICINARUM E RADICE FERM 34D DIL. D5 (HAB, VS. 34D)1.00gram(s)10.00millilitre(s)
-
LEONTOPODIUM ALPINUM E PLANTA TOTA FERM 36 DIL. D3 (HAB, VS. 36)1.00gram(s)10.00millilitre(s)
-
GRANIT DIL. D9 (HAB, VS. 6)1.00gram(s)10.00millilitre(s)
-
GELSEMIUM SEMPERVIRENS E RHIZOMA FERM 35B DIL. D3 (HAB, VS. 35B)1.00gram(s)10.00millilitre(s)
-
ACONITUM NAPELLUS E TUBERE FERM 33C DIL. D5 (HAB, VS. 33C)1.00gram(s)10.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Legal status of supply:
-
Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Germany
Package description:
- Available only in German
Additional information
Entitlement type:
-
Homeopathic Registration
Marketing authorisation holder:
- SaluVet GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Wala-Heilmittel GmbH
Responsible authority:
- Federal Office Of Consumer Protection And Food Safety
Authorisation number:
- 402712.00.00
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.
German (PDF)
Published on: 10/01/2025
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
German (PDF)
Published on: 10/01/2025
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