Veterinary Medicines

RemaTuss - Hustenglobuli für Tiere

Authorised
  • AMMONIUM CARBONICUM C200
  • BRYONIA C200
  • DACTYLOPIUS COCCUS C200
  • DROSERA C200
  • RUMEX CRISPUS C200
  • EUSPONGIA OFFICINALIS C200
  • STANNUM METALLICUM C200
Download as PDF

Product identification

Medicine name:
RemaTuss - Hustenglobuli für Tiere
Active substance:
  • AMMONIUM CARBONICUM C200
  • BRYONIA C200
  • DACTYLOPIUS COCCUS C200
  • DROSERA C200
  • RUMEX CRISPUS C200
  • EUSPONGIA OFFICINALIS C200
  • STANNUM METALLICUM C200
Target species:
  • Cattle
  • Dog
  • Goat
  • Sheep
  • Horse
  • Cat
  • Rabbit
  • Ferret
  • Small rodents
  • Pig
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • AMMONIUM CARBONICUM C200
    1.43
    milligram(s)
    /
    1.00
    gram(s)
  • BRYONIA C200
    1.43
    milligram(s)
    /
    1.00
    gram(s)
  • DACTYLOPIUS COCCUS C200
    1.43
    milligram(s)
    /
    1.00
    gram(s)
  • DROSERA C200
    1.43
    milligram(s)
    /
    1.00
    gram(s)
  • RUMEX CRISPUS C200
    1.43
    milligram(s)
    /
    1.00
    gram(s)
  • EUSPONGIA OFFICINALIS C200
    1.43
    milligram(s)
    /
    1.00
    gram(s)
  • STANNUM METALLICUM C200
    1.43
    milligram(s)
    /
    1.00
    gram(s)
Pharmaceutical form:
  • Pillules
Withdrawal period by route of administration:
  • Oral use
    • Cattle
      • Meat and offal
        0
        day
      • Milk
        0
        hour
    • Goat
      • Meat and offal
        0
        day
      • Milk
        0
        hour
    • Sheep
      • Meat and offal
        0
        day
      • Milk
        0
        hour
    • Horse
      • Meat and offal
        0
        day
      • Milk
        0
        hour
    • Rabbit
      • Meat and offal
        0
        day
    • Pig
      • Meat and offal
        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:
  • Austria
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:
  • Remedia Homoeopathie Mag. pharm. Robert Muentz Ges.m.b.H.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Remedia Homoeopathie Mag. pharm. Robert Muentz Ges.m.b.H.
Responsible authority:
  • Austrian Agency For Health And Food Safety
Authorisation number:
  • 840705
Date of authorisation status change:

Documents

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 1/10/2024
Updated on: 13/01/2026
Download

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: 1/10/2024
Updated on: 13/01/2026
Download

Labelling

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 1/10/2024
Updated on: 13/01/2026
Download

at-puar-600000091857-np-remaetuess-de.pdf

German (PDF)
Published on: 12/03/2025
Updated on: 13/01/2026
Download