1. 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. (1) product name and brand name, if any, as stipulated in Subsection A of 21.18.3.9 NMAC;
   2. (2) if a drug is used, label as stipulated in Subsection B of 21.18.3.9 NMAC;
   3. (3) purpose statement as stipulated in Subsection C of 21.18.3.9 NMAC;
   4. (4) guaranteed analysis as stipulated in Subsection D of 21.18.3.9 NMAC;
   5. (5) feed ingredients as stipulated in Subsection E of 21.18.3.9 NMAC and in 21.18.3.12 NMAC;
   6. (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. (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. (8) quantity statement.

2. B. PRINCIPAL DISPLAY PANEL:

   1. (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. (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."
3. C. None of the information required by 21.18.3.8 NMAC shall be subordinated or obscured by other statements or designs.

4. 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. (1) the name and address of the manufacturer;
   2. (2) the name and address of the purchaser;
   3. (3) the date of sale or delivery;
   4. (4) the customer-formula feed name and brand name if any;
   5. (5) the product name and net quantity of each registered commercial feed and each other ingredient used in the mixture;
   6. (6) the direction for use and precautionary statements as required by 21.18.3.13 NMAC and 21.18.3.14 NMAC.

   7. (7) If a drug containing product is used:

      1. (a) the purpose of the medication (claim statement);
      2. (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.

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