Commission Implementing Regulation (EU) 2016/2074 of 25 November 2016 amending Regulation (EU) No 37/2010 as regards the substance aluminium salicylate, basic (Text with EEA relevance)
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Changes over time for: Commission Implementing Regulation (EU) 2016/2074 (Annexes only)
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Point in time view as at 31/01/2020.
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There are currently no known outstanding effects for the Commission Implementing Regulation (EU) 2016/2074.
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ANNEXU.K.
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
| 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 | |
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