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1. The label or mark shall give—
(a)in the case of any additive,
(i)the name of the additive;
(ii)the name or business name and the address or registered business address of the person responsible within the European Economic Community for the particulars referred to in this Part;
(b)in the case of vitamin E,
(i)the alpha-tocopherol level as acetate;
(ii)an indication of the period during which that level will remain present;
(c)in the case of any vitamin other than vitamin E, or any added provitamin or substance having a similar effect,
(i)the active substance level;
(ii)an indication of the period during which that level will remain present;
(d)in the case of any trace element, colourant (including pigment), preservative or other additive not specified above, the active substance level.
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