8 CCR 1202-6 Part 3 - Label Format

3.1. Commercial feed, other than customer-formula feed, shall be labeled with the information prescribed in this Part on the principal display panel of the product and in the following format:
3.1.1. Product name and brand name, if any, as stipulated in Part 4.1.1.
3.1.2. If a drug is used, label as stipulated in Part 4.1.2.
3.1.3. Purpose Statement as stipulated in Part 4.1.3.
3.1.4. Guaranteed analysis as stipulated in Part 4.1.4.
3.1.5. Feed ingredients as stipulated in Part 4.1.5.
3.1.6. Directions for use and precautionary statements as stipulated in Part 4.1.6.
3.1.7. Name and principal mailing address of the manufacturer or person responsible for distributing the feed as stipulated Part 4.1.7.
3.1.8. Quantity Statement.
3.1.9. The date of manufacture, processing, packaging, or repackaging or a code that permits the determination of the date.
3.2. The information required in Parts 3.1.1 through 3.1.5, 3.1.7 and 3.1.8 must appear in its entirety on one side of the label or on one side of the container.
3.3. The information required by Part 3.1.6 shall be displayed in a prominent place on the label or container but not necessarily on the same side as the above information. When the information required by Part 3.1.6 is placed on a different side of the label or container, it must 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 Part 3 shall be subordinated or obscured by other statements or designs.
3.4. Customer-formula feed shall be accompanied with the information prescribed in this Part using labels, invoice, delivery ticket, or other shipping document bearing the following information.
3.4.1. The name and address of the manufacturer.
3.4.2. The name and address of the purchaser.
3.4.3. The date of sale or delivery.
3.4.4. The customer-formula feed name and brand name if any.
3.4.5. The product name and net quantity of each registered commercial feed and each other ingredient used in the mixture.
3.4.6. The direction for use and precautionary statements as required by Parts 8 and 9.
3.4.7. If a drug containing product is used:
3.4.7.1. The purpose of the medication (claim statement).
3.4.7.2. The established name of each active drug ingredient and the level of each drug used in the final mixture expressed in accordance with Part 5.4.

Notes

8 CCR 1202-6 Part 3
38 CR 05, March 10, 2015, effective 3/30/2015 39 CR 05, March 10, 2016, effective 3/30/2016 39 CR 23, December 10, 2016, effective 12/30/2016 40 CR 20, October 25, 2017, effective 11/30/2017 43 CR 22, November 25, 2020, effective 12/15/2020 45 CR 22, November 25, 2022, effective 12/15/2022

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