Section 4.1-41-06 - Commercial feed - Label - ContentExcept as provided in section 4.1-41-07, any commercial feed that is distributed in this state must be labeled. The label must include:
1. The product's name, including any brand name under which the product is distributed;2. The product's weight, volume, or quantity, as appropriate;3. A guaranteed analysis expressed on an "as is" basis as determined by the commissioner to adequately advise the consumer of the composition and contents of the commercial feed or to support claims made in the labeling. The composition and contents of the commercial feed must be determinable by laboratory tests, such as the methods published by the association of official analytical chemists international;4. Unless waived by the commissioner in the interest of consumers, the commonly accepted name of each ingredient or, if permitted by the commissioner, a collective term for a group of ingredients that perform a similar function;5. The name and principal mailing address of the manufacturer or the distributor;6. Directions for the safe and effective use of all commercial feed containing drugs and those determined by the commissioner as being necessary; and7. Any precautionary statements recommended by the commissioner to ensure the safe and effective use of the feed.Amended by S.L. 2019 , ch. 71( HB 1134 ), § 5, eff. 8/1/2019.Added by S.L. 2017 , ch. 68( SB 2028 ), § 7, eff. 7/1/2017.