N.D. Cent. Code § 4.1-41-07 (2025)
Any customer-formula feed that is distributed in this state must be labeled.
1. The label must include: a. The name and address of the manufacturer; b. The name and address of the purchaser; c. The date of delivery; d. The product's name; e. The quantity statement of each ingredient, including commercial feed; f. Directions for the safe and effective use of all customer-formula feed containing drugs and those determined by the commissioner as being necessary; and g. Any precautionary statement recommended by the commissioner to ensure the safe and effective use of the feed.
2. If the feed contains drugs, the label must also include: a. The purpose of each drug; b. The weight, volume, or quantity, as appropriate, of each drug; and c. The name of each active ingredient.