HB3574 HFLR Page 1 BOLD FACE denotes Committee Amendments. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 HOUSE OF REPRESENTATIVES - FLOOR VERSION STATE OF OKLAHOMA 2nd Session of the 59th Legislature (2024) HOUSE BILL 3574 By: Pae of the House and Prieto of the Senate AS INTRODUCED An Act relating to public health and safety; amendin g 63 O.S. 2021, Section 1 -1432.4, which relates to the Oklahoma Kratom Consumer Protecti on Act; requiring additional information when labeling kratom products; and providing an effective date . BE IT ENACTED BY THE PEOPLE OF THE STATE OF OKLAHOM A: SECTION 1. AMENDATORY 63 O.S. 2021, Section 1 -1432.4, is amended to read as follows: Section 1-1432.4 A. A vendor shall not prepare, distribute, sell or expose for sale any of the f ollowing: 1. A kratom product that is adult erated with a nonkra tom substance. A kratom product is adulterated with a nonkratom substance if the kratom product is mixed or packed with a nonkratom substance and that substance affects the quality or streng th of the HB3574 HFLR Page 2 BOLD FACE denotes Committee Amendments. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 kratom product to such a degree as to render the kratom product injurious to a consumer; 2. A kratom product that is contaminated with a dangerou s nonkratom substance. A kratom product is contaminated with a dangerous nonkratom substance if th e kratom product contains a substance that is not safe for human c onsumption; 3. A kratom product containing a level of 7 -hydroxymitragynine in the alkaloid fraction that is greater than two percent (2%) of the alkaloid composition of the product; 4. A kratom product containing any synthetic alkaloi d including synthetic mitragynine, synthetic 7 -hydroxymitragynine or any other synthetically derived compounds of the kratom plant; or 5. A kratom product containing any controlled substance listed in the Uniform Controlled Dangerous Substances Act, unles s the product is compounded by a licensed pharmacist with the controlled substance dispensed in accordance wit h a valid prescription. B. Kratom products shall be accompanied by a label, or a quick response (QR) code on the product label linked to a websit e, bearing the following information prior to its sale in this state: 1. A list of the ingredients, which shall include the common or usual name of each ingredient used in the manufacture of the product, listed in descending order of predominance; 2. That the sale or transfer of kratom to a person under eighteen (18) years of age is prohi bited; HB3574 HFLR Page 3 BOLD FACE denotes Committee Amendments. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 3. The amount of mitragynine and 7-hydroxymitragynine contained in the product; 4. The amount of mitragyni ne and 7-hydroxymitragynine contained in packaging for the product; 5. The name and the principal street address of the vendor or the person responsible for distrib uting the product; 6. The suggested Clear and adequate directions for the consumption and safe and effective use of the such product, including the recommended serving size, the number of serving s in the container, the num ber of servings that can be safe ly consumed in a day, and the time frame within which safe consumption should occur; and 7. Any precautionary state ments as to the safety and effectiveness of the product , including a warning that a consumer should consult his or her physician on questio ns about use of kratom, and state that the kratom product is not intended to "diagnose, treat, cure , or prevent any disease "; and 8. A statement that a kratom product label is prohibited from making any therapeutic claims unless approved by the United States Food and Drug Administration. C. A vendor may not distribute, sell or expose for sale a kratom product to an individual under eighteen (18) years of age. HB3574 HFLR Page 4 BOLD FACE denotes Committee Amendments. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 D. Upon request by the State Department of Health, the vendor shall provide test results from a United States-based testing facility to confirm the items listed on the product label. SECTION 2. This act shall become effective November 1, 2024. COMMITTEE REPORT BY: COMMITTEE ON ALCOHOL, TOBACCO AND CONTROLLED SUBSTANCES, dated 02/14/2024 - DO PASS, As Coauthored.