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.
2. The label or mark may give, in addition to the name used in relation to any additive in the Table to Schedule 4—
(a)the trade name of the additive and its EEC number;
(b)the name or business name and the address or registered business address of the manufacturer;
(c)directions for use, including any appropriate safety recommendation.