Article 1
The Annex to Regulation (EU) No 37/2010 is amended as set out in the Annex to this Regulation.
Commission Implementing Regulation (EU) No 1186/2012 of 11 December 2012 amending the Annex to Regulation (EU) No 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance phoxim Text with EEA relevance
Commission Implementing Regulation (EU) No 1186/2012 of 11 December 2012 amending the Annex to Regulation (EU) No 37/2010 on pharmacologically active substances and their classification regarding maximum residue limits in foodstuffs of animal origin, as regards the substance phoxim Text with EEA relevance
Data as of 2026-07-04 · Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails. · Read the official text ↗
Article 2
This Regulation shall enter into force on the third day following that of its publication in the Official Journal of the European Union . It shall apply from 13 February 2013.
Supplementary provisions
ANNEXSupplementary provisions
ANNEX The entry corresponding to phoxim in Table 1 of the Annex to Regulation (EU) No 37/2010 is replaced by the following: Pharmacologically active substance Marker residue Animal Species MRL Target Tissues Other Provisions (according to Article 14(7) of Regulation (EC) No 470/2009) Therapeutic classification ‘Phoxim Phoxim All food-producing species except fin fish. 25 μg/kg Muscle For porcine and poultry species the fat MRL relates to “skin and fat in natural proportions”. Not for use in animals from which milk is produced for human consumption. Antiparasitic agents/Agents against ectoparasites.’ 550 μg/kg Fat 50 μg/kg Liver 30 μg/kg Kidney 60 μg/kg Eggs
Source: EUR-Lex (Publications Office of the EU), © European Union, reuse permitted under Commission Decision 2011/833/EU.
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