Schedule 5 Medicated feedingstuffs and specified feed additives
United Kingdom
- 1Scope and interpretation
- 2Enforcement of Regulation (EC) No 178/2002
- 3Enforcement of Regulation (EC) No 1831/2003
- 4Enforcement of Regulation (EU) 2017/625
- 5Enforcement of Regulation (EC) No 183/2005
- 6Enforcement of Regulation (EC) No 767/2009
- 7Authorisation of manufacturers and distributors of feedingstuffs containing medicinal premixes
- 8Incorporation of a medicinal premix into an intermediate feedingstuff
- 9Top dressing
- 10Incorporation of a medicinal premix into feedingstuffs
- 11Additional record keeping requirements relating to medicinal premixes
- 12Labelling an intermediate feedingstuff containing a medicinal premix
- 13Labelling of feedingstuffs containing a specified feed additive
- 14Labelling of feedingstuffs containing a medicinal premix
- 15Supply of specified feed additives
- 16Supply of intermediate feedingstuff or specified feed additive
- 17Supply of a complementary feedingstuff
- 18Supply of feedingstuffs containing a medicinal premix
- 19Medicated feedingstuff prescriptions for feedingstuffs containing a medicinal premix
- 20Writing the medicated feedingstuff prescription
- 21Possession
- 22Sampling and analysis
- 22ASampling for cross-contamination
- 23Storage
- 24Packages and other containers
- 25Transport
- 26Possession, placing on the market and use of feedingstuffs
- 26AUnused and expired medicated feedingstuffs
- 27Imports from third countries
- 28Trade between countries
- 29Import for incorporation into intermediate feedingstuffs or feedingstuffs for export
- 30Animals on domestic premises
- 31Offences