Veterinary Medicine Information website

Novaderma 660 mg/g + 7.7 mg/g cutaneous paste for horses, cattle and sheep

Authorised
  • Methyl salicylate
  • Salicylic acid
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Product identification

Medicine name:
Novaderma 660 mg/g + 7.7 mg/g cutaneous paste for horses, cattle and sheep
Active substance:
  • Methyl salicylate
  • Salicylic acid
Target species:
  • Cattle
  • Sheep
  • Horse
Route of administration:
  • Cutaneous use

Product details

Active substance and strength:
  • Methyl salicylate
    7.70
    milligram(s)
    /
    1.00
    gram(s)
  • Salicylic acid
    660.00
    milligram(s)
    /
    1.00
    gram(s)
Pharmaceutical form:
  • Cutaneous paste
Withdrawal period by route of administration:
  • Cutaneous use
    • Cattle
      • Milk
        24
        hour
      • Meat and offal
        1
        day
    • Sheep
      • Milk
        24
        hour
      • Meat and offal
        1
        day
    • Horse
      • Milk
        24
        hour
      • Meat and offal
        1
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QD02AF
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • France
Package description:
  • (ID1) 500 gram(s): Box (cardboard) with 1 Jar (polypropylene) with 500 gram(s), closed with Schraubdeckel (polypropylene)

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Hybrid application – bioavailability studies cannot be used to demonstrate bioequivalence (Article 19(1)(b) of Regulation (EU) 2019/6)
Marketing authorisation holder:
  • Wirtschaftsgenossenschaft deutscher Tieraerzte eG
Marketing authorisation date:
Manufacturing sites for batch release:
  • Wirtschaftsgenossenschaft deutscher Tieraerzte eG
Responsible authority:
  • French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
  • FR/V/6781929 8/2026
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0349/001
Concerned member states:
  • Austria
  • Belgium
  • Czechia
  • France
  • Hungary
  • Ireland
  • Italy
  • Luxembourg
  • Netherlands
  • Poland
  • Portugal
  • United Kingdom (Northern Ireland)

Documents

Combined File of all Documents

English (PDF)
Published on: 8/05/2026
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Summary of Product Characteristics

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French (PDF)
Published on: 8/05/2026
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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: 8/05/2026
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