Nothing in this part 5 prohibits or limits the use of any material used in the packaging of a product that is regulated as a drug, medical device, or dietary supplement by the food and drug administration in the United States department of health and human services under the 'Federal Food, Drug, and Cosmetic Act', 21 U.S.C. sec. 321 et seq., as amended, or any equipment and materials used to manufacture such products.Added by 2021 Ch. 440,§2, eff. 7/6/2021.L. 2021: Entire part added, (HB 21-1162), ch. 2916, p. 2916, § 2, effective July 6.
Colorado Legal Code