new text begin Enforcement. new text end

new text begin (a) A product sold under this section shall be considered an adulterated drug if: new text end

new text begin (1) it consists, in whole or in part, of any filthy, putrid, or decomposed substance; new text end

new text begin (2) it has been produced, prepared, packed, or held under unsanitary conditions where it may have been rendered injurious to health, or where it may have been contaminated with filth; new text end

new text begin (3) its container is composed, in whole or in part, of any poisonous or deleterious substance that may render the contents injurious to health; new text end

new text begin (4) it contains any color additives or excipients that have been found by the FDA to be unsafe for human or animal consumption; or new text end

new text begin (5) it contains an amount or percentage of cannabinoids that is different than the amount or percentage stated on the label. new text end

new text begin (b) A product sold under this section shall be considered a misbranded drug if the product's labeling is false or misleading in any manner or in violation of the requirements of this section. new text end

new text begin (c) The board's authority to issue cease and desist orders under section 151.06; to embargo adulterated and misbranded drugs under section 151.38; and to seek injunctive relief under section 214.11, extends to any violation of this section. new text end