
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 twentieth day following that of its publication in the Official Journal of the European Union.
It shall apply from 25 January 2017.
This Regulation shall be binding in its entirety and directly applicable in all Member States.Done at Brussels, 25 November 2016.
For the Commission
The President
Jean-Claude JUNCKER
ANNEX

In Table 1 of the Annex to Regulation (EU) No 37/2010, the entry for the substance 'aluminium salicylate, basic 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
‘aluminium salicylate, basic Salicylic acid Bovine,caprine,Equidae,rabbit 200 μg/kg500 μg/kg1 500 μg/kg1 500 μg/kg MuscleFatLiverKidney NO ENTRY Antidiarrheal and intestinal anti-inflammatory agents’
Bovine,caprine,Equidae 9 μg/kg Milk
 NOT APPLICABLE All food producing species except bovine, caprine, Equidae, rabbit and fin fish No MRL required NOT APPLICABLE For topical use only 
