Restitutionsfluid, oplossing voor cutaan gebruik voor herkauwers en eenhoevigen
Restitutionsfluid, oplossing voor cutaan gebruik voor herkauwers en eenhoevigen
Authorised
- D-camphor
- Symphytum officinale root, water decoctum (20:1)
- Tincture from fructus capsici, flores arnicae, rhizoma symphiti and semen sinapis. Extraction solvent: isopropyl alcohol 60%
- Ammonia
Product identification
Medicine name:
Restitutionsfluid, oplossing voor cutaan gebruik voor herkauwers en eenhoevigen
Active substance:
- D-camphor
- Symphytum officinale root, water decoctum (20:1)
- Tincture from fructus capsici, flores arnicae, rhizoma symphiti and semen sinapis. Extraction solvent: isopropyl alcohol 60%
- Ammonia
Target species:
-
Ruminant
-
Equid
Route of administration:
-
Cutaneous use
Product details
Active substance and strength:
-
D-camphor9.00milligram(s)1.00gram(s)
-
Symphytum officinale root, water decoctum (20:1)0.20millilitre(s)1.00millilitre(s)
-
Tincture from fructus capsici, flores arnicae, rhizoma symphiti and semen sinapis. Extraction solvent: isopropyl alcohol 60%0.55millilitre(s)1.00millilitre(s)
-
Ammonia0.15millilitre(s)1.00millilitre(s)
Pharmaceutical form:
-
Cutaneous solution
Withdrawal period by route of administration:
-
Cutaneous use
-
Ruminant
-
Milkno withdrawal periodzero days
-
Meat and offalno withdrawal periodzero days
-
-
Equid
-
Meat and offalno withdrawal periodzero days
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QV03AX
Legal status of supply:
-
Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Netherlands
Package description:
- Available only in Dutch
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- EUROstyle B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- SaluVet GmbH
Responsible authority:
- Medicines Evaluation Board
Authorisation number:
- REG NL 5630
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
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Dutch (PDF)
Published on: 24/02/2022
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