North Dakota § 4.1-41-07 Customer-formula feed - Label - Content

North Dakota Statutes

§ 4.1-41-07 — Customer-formula feed - Label - Content

North Dakota § 4.1-41-07

Title 4.1Agriculture

Ch. 4.1-41Commercial Feed

This text of North Dakota § 4.1-41-07 (Customer-formula feed - Label - Content) is published on Counsel Stack Legal Research, covering North Dakota primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook

N.D. Cent. Code § 4.1-41-07 (2026).

Text

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.

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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.