Commission Regulation (EU) No 914/2010 of 12 October 2010 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 sodium salicylate Text with EEA relevance

• CELEX: Regulation (EU) No 914/2010
• Articles: 3

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 its publication in the Official Journal of the European Union .

It shall apply from 12 December 2010.

Schedules & Appendices

ANNEX

ANNEX

The entry Sodium salicylate in Table 1 of the Annex to Regulation (EU) No 37/2010 shall be 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.

Provisional maximum residue limits shall expire on 1 January 2015.

Anti-inflammatory agents/Non-steroidal anti-inflammatory agents’

2 500  μg/kg

Skin and fat

200  μg/kg

Liver

150  μg/kg

Kidney