Section 355 IAC 6-1-2 - Label formatAuthority: IC 15-19-7-34
Affected: IC 15-19-7
Sec. 2.
(a) Commercial feed, other than custom-mixed feed, shall be labeled with the information prescribed in this rule on the principal display panel of the product and in the following format:(1) Product name and brand name, if any, as stipulated in section 3(a)(1) of this rule.(2) If a drug is used, label as stipulated in section 3(a)(2) of this rule.(3) Purpose statement as stipulated in section 3(a)(3) of this rule.(4) Guaranteed analysis as stipulated in section 3(a)(4) of this rule.(5) Feed ingredients as stipulated in section 3(a)(5) of this rule.(6) Directions for use and precautionary statements as stipulated in section 3(a)(6) of this rule.(7) Name and principal mailing address of the manufacturer or person responsible for distributing the feed as stipulated in section 3(a)(7) of this rule.(b) The following requirements apply to labeling:(1) The information required in subsection (a)(1) through (a)(5), (a)(7), and (a)(8) must appear in its entirety on one (1) side of the label or on one (1) side of the container.(2) The information required by subsection (a)(6) shall be displayed in a prominent place on the label or container but not necessarily on the same side as the information in subdivision (1). When the information required by subsection (a)(6) is placed on a different side of the label or container, it shall be referenced on the front side with a statement, such as "See back of label for directions for use.". None of the information required by this section shall be subordinated or obscured by other statements or designs.(c) Custom mixed feed shall be accompanied with the information prescribed in this rule using labels, invoice, delivery ticket, or another distribution 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 custom mixed feed name and brand name if any.(5) The product name and net quantity of each commercial feed and each other ingredient used in the mixture.(6) The direction for use and precautionary statements as required by sections 7 and 8 of this rule.(7) If a drug containing product is used, the:(A) purpose of the medication (claim statement); and(B) established name of each active drug ingredient and the level of each drug used in the final mixture expressed in accordance with section 4(d) of this rule.State Chemist of the State of Indiana; 355 IAC 6-1-2; filed Apr 4, 2002, 9:26 a.m.: 25 IR 2444; readopted filed Nov 12, 2008, 11:24 a.m.: 20081203-IR-355080677RFAReadopted filed 10/17/2014, 9:27 a.m.: 20141112-IR-355140344RFAReadopted filed 10/26/2020, 10:26 a.m.: 20201125-IR-355200460RFA