1. (1) To register a cannabinoid product, a registrant shall submit an application to the department that includes the following information:

   1. (a) a complete copy of the label as it will appear on the product in a legible format;
   2. (b) a COA from the department's analytical laboratory for the amount of any THC analogs present in the sample; and
   3. (c) a COA from the department's analytical laboratory or a third party testing laboratory for adulterants presence as required in this rule.
2. (2) The department may deny registration for an incomplete application.

3. (3) The department requires a new registration for any of the following changes:

   1. (a) in the cannabinoid product ingredients;
   2. (b) to the directions for use; and
   3. (c) of the name for the product.
4. (4) Other changes may not require a new registration but the registrant shall submit copies of each label change to the department as soon as they are effective.
5. (5) The registrant is responsible for the accuracy and completeness of information submitted.

6. (6) The department may not register a cannabinoid product if the product:

   1. (a) uses the cannabinoid as a food additive; or

   2. (b) is represented for use as a conventional food, with the exception of:

      1. (i) a gummy if the gummy is shaped as a gelatinous cube or gelatinous rectangular cuboid or in another basic geometric shape and not in a shape that could be considered appealing to children such as a star shape, fruit, or animal shape; or
      2. (ii) a liquid suspension under two ounces.

KEY: CBD labeling, CBD products, cannabinoid product registration; cannabinoid product labeling; cannabinoid testing, cannabinoid COA; violations

Date of Last Change: October 10, 2025

Authorizing, and Implemented or Interpreted Law: 4-41-403(1); 4-41-402(2); 4-41-103(4)