{"topic_id":"eu_reg_2020_354_a_004","category":"eu-2026","context":"---\ntopic_id: eu_reg_2020_354_a_004\ncategory: EU-REG-2020-354\ntitle: Part A - this shall be established in the column ‘other provisions’ o\nlang: en\nsource: reg_2020_354_consolidated.pdf\ndate_parsed: 2026-07-18\ntokens_estimated: 1466\nextra: {\"part\": \"A\", \"section\": 2, \"consolidated_version\": \"2025-04-22\"}\n---\n\n# Part A - this shall be established in the column ‘other provisions’ o\n\nthis shall be established in the column ‘other provisions’ of the respective\nfeed. Such feed shall exclusively contain, including a potential coating, feed\nmaterials and feed additives, unless detailed otherwise in the respective entry.\nIt is recommended that feed intended for individual oral administration is\nadministered by a veterinarian or any other competent person.\n(1) Regulation (EC) No 1831/2003 of the European Parliament and of the Council of\n22 September 2003 on additives for use in animal nutrition (OJ L 268, 18.10.2003,\np. 29).\n(2) Directive 2004/48/EC of the European Parliament and of the Council of 29 April 2004\non the enforcement of intellectual property rights (OJ L 157, 30.4.2004, p. 45).\n\n02020R0354 — EN — 22.04.2025 — 002.001 — 4\n▼B\n10. When a feed intended for particular nutritional purposes is placed on the\nmarket in the form of a bolus, being a feed material or complementary feed\nintended for individual oral administration with retarding release, i.e. more\nthan 24 hours, of the compounds, the labelling of such feed shall, if\napplicable, mention for each feed additive for which a maximum content\nin complete feed is fixed the maximum period of continuous release of the\nbolus and the daily release rate. The feed business operator which is placing\na bolus on the market shall have the proof that the daily available feed\nadditive level in the digestive tract will not exceed, if applicable, the\nmaximum content of the additive established per kg complete feed during\nthe whole feeding period (retarding release effect). Such proof should be\nbased on a peer reviewed methodology or in-house analysis.\n11. In case of intended uses for which in column 2 a concentration of certain\nfeed additives higher than 100 times the relevant fixed maximum content in\ncomplete feed is allowed for complementary feed, the concentration of those\nfeed additives shall not be higher than 500 times the relevant fixed maximum\ncontent in complete feed, except in the case of boluses as referred to in\npoint 10. The incorporation of such complementary feed into the animal's\ndiet shall ensure that the uptake of the animal complies with the fixed\nmaximum content in complete feed.\n\n▼B\n","sources":[],"tokens_estimated":1466,"generated_at":null,"tip":"Use /api/v1/topics to discover more topics. /api/v1/nutrient for precise single-point queries. /api/v1/cross_compare for 2-3 standard comparisons."}