N.M. Admin. Code § 21.18.3.8

Current through Register Vol. 35, No. 21, November 5, 2024

Section 21.18.3.8 - LABEL FORMAT

A. Commercial feed, other than customer-formula feed, shall be labeled with the information prescribed in this regulation on the principal display panel of the product and in the following format:

(1) product name and brand name, if any, as stipulated in Subsection A of 21.18.3.9 NMAC;

(2) if a drug is used, label as stipulated in Subsection B of 21.18.3.9 NMAC;

(3) purpose statement as stipulated in Subsection C of 21.18.3.9 NMAC;

(4) guaranteed analysis as stipulated in Subsection D of 21.18.3.9 NMAC;

(5) feed ingredients as stipulated in Subsection E of 21.18.3.9 NMAC and in 21.18.3.12 NMAC;

(6) directions for use and precautionary statements as stipulated in Subsection F of 21.18.3.9 NMAC and in 21.18.3.13 NMAC;

(7) name and principal mailing address of the manufacturer or person responsible for distributing the feed as stipulated in Subsection G of 21.18.3.9 NMAC;

(8) quantity statement.

B. PRINCIPAL DISPLAY PANEL:

(1) The information as required in Paragraphs (1), (2), (3), and (8) of Subsection A of 21.18.3.8 NMAC must appear in its entirety on the principal display panel.

(2) The information required by Paragraphs (4), (5), (6), and (7) of Subsection A of 21.18.3.8 NMAC shall be displayed in a prominent place on the feed tag or label, but not necessarily on the principal display panel. When a precautionary statement required by Paragraph (6) of Subsection A of 21.18.3.8 NMAC does not appear on the principal display panel, it must be referenced on the principal display panel with a statement such as "See back of label for precautions."

C. None of the information required by 21.18.3.8 NMAC shall be subordinated or obscured by other statements or designs.

D. Customer-formula feed shall be accompanied with the information prescribed in this regulation using labels, invoice, delivery ticket, or other shipping document bearing the following information:

(1) the name and address of the manufacturer;

(2) the name and address of the purchaser;

(3) the date of sale or delivery;

(4) the customer-formula feed name and brand name if any;

(5) the product name and net quantity of each registered commercial feed and each other ingredient used in the mixture;

(6) the direction for use and precautionary statements as required by 21.18.3.13 NMAC and 21.18.3.14 NMAC.

(7) If a drug containing product is used:

(a) the purpose of the medication (claim statement);

(b) the established name of each active drug ingredient and the level of each drug used in the final mixture expressed in accordance with Subsection D of 21.18.3.10 NMAC.

N.M. Admin. Code § 21.18.3.8

21.18.3.8 NMAC - Rp, 21.18.3.9 & 10 NMAC, 9/30/2013