
Article 1 
The Annex to Regulation (EU) No 37/2010 is amended as set out in the Annex to this Regulation.
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.
This Regulation shall be binding in its entirety and directly applicable in all Member States.Done at Brussels, 12 December 2012.
For the Commission
The President
José Manuel BARROSO
ANNEX

The entry corresponding to sodium salicylate 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
‘Sodium salicylate NOT APPLICABLE Bovine, porcine No MRL required NOT APPLICABLE For oral use.Not for use in animals from which milk is produced for human consumption. NO ENTRY
All food-producing species except fin fish No MRL required NOT APPLICABLE For topical use only.
Salicylic acid Turkey 400 μg/kg Muscle Not for use in animals producing eggs for human consumption. Anti-inflammatory agents/Non-steroidal anti-inflammatory agents’
2 500 μg/kg Skin and fat in natural proportions
200 μg/kg Liver
150 μg/kg Kidney
