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Commission Implementing Regulation (EU) 2015/1308 of 29 July 2015 amending Regulation (EU) No 37/2010 as regards the substance ‘aluminium salicylate, basic’ (Text with EEA relevance)

Implementing Regulation (EU) 2015/1308 · Regulation · 3 articles

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 1

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The Annex to Regulation (EU) No 37/2010 is amended as set out in the Annex to this Regulation.

Article 2

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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 28 September 2015.

Supplementary provisions

ANNEXSupplementary provisions

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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/kg 500 μg/kg 1 500 μg/kg 1 500 μg/kg Muscle Fat Liver Kidney Provisional MRLs expire on 31 December 2016. Antidiarrhoeal 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.

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Source: EUR-Lex (Publications Office of the EU), © European Union, reuse permitted under Commission Decision 2011/833/EU.

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