1 STATE OF OKLAHOMA
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2 2nd Session of the 59th Legislature (2024)
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3 SENATE BILL 1639 By: Prieto
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6 AS INTRODUCED
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7 An Act relating to kratom products; amending 63 O.S.
7 2021, Section 1-1432.4, which relates to labeling
8 requirements; modifying and adding labeling
8 requirements for kratom products; and providing an
9 effective date.
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12 BE IT ENACTED BY THE PEOPLE OF THE STATE OF OKLAHOMA:
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13 SECTION 1. AMENDATORY 63 O.S. 2021, Section 1-1432.4, is
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14 amended to read as follows:
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15 Section 1-1432.4. A. A vendor shall not prepare, distribute,
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16 sell or expose for sale any of the following:
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17 1. A kratom product that is adulterated with a nonkratom
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18 substance. A kratom product is adulterated with a nonkratom
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19 substance if the kratom product is mixed or packed with a nonkratom
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20 substance and that substance affects the quality or strength of the
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21 kratom product to such a degree as to render the kratom product
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22 injurious to a consumer;
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23 2. A kratom product that is contaminated with a dangerous
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24 nonkratom substance. A kratom product is contaminated with a
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1 dangerous nonkratom substance if the kratom product contains a
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2 substance that is not safe for human consumption;
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3 3. A kratom product containing a level of 7-hydroxymitragynine
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4 in the alkaloid fraction that is greater than two percent (2%) of
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5 the alkaloid composition of the product;
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6 4. A kratom product containing any synthetic alkaloid including
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7 synthetic mitragynine, synthetic 7-hydroxymitragynine or any other
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8 synthetically derived compounds of the kratom plant; or
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9 5. A kratom product containing any controlled substance listed
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10 in the Uniform Controlled Dangerous Substances Act, unless the
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11 product is compounded by a licensed pharmacist with the controlled
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12 substance dispensed in accordance with a valid prescription.
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13 B. Kratom products shall be accompanied by a label, or a quick
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14 response (QR) code on the product label linked to a website, bearing
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15 the following information prior to its sale in this state:
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16 1. A list of the ingredients, which shall include the common or
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17 usual name of each ingredient used in the manufacture of the
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18 product, listed in descending order of predominance;
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19 2. That the sale or transfer of kratom to a person under
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20 eighteen (18) years of age is prohibited;
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21 3. The amount of mitragynine and 7-hydroxymitragynine contained
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22 in the product;
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23 4. The amount of mitragynine and 7-hydroxymitragynine contained
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24 in packaging for the product;
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1 5. The name and the principal street address of the vendor or
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2 the person responsible for distributing the product;
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3 6. The suggested Clear and adequate directions for the
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4 consumption of and safe and effective use of the product, including
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5 the recommended serving size, the number of servings in the
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6 container, the number of servings that can be safely consumed in a
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7 day, and the time frame within which safe consumption should occur;
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8 and
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9 7. Any precautionary statements as to the safety and
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10 effectiveness of the product, including a warning that a consumer
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11 should consult his or her physician on questions about use of kratom
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12 and a statement that the kratom product is not intended to
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13 “diagnose, treat, cure, or prevent any disease”; and
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14 8. A statement that a kratom product label is prohibited from
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15 making any therapeutic claims unless approved by the United States
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16 Food and Drug Administration.
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17 C. A vendor may not distribute, sell or expose for sale a
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18 kratom product to an individual under eighteen (18) years of age.
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19 D. Upon request by the State Department of Health, the vendor
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20 shall provide test results from a United States-based testing
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21 facility to confirm the items listed on the product label.
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22 SECTION 2. This act shall become effective November 1, 2024.
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24 59-2-2988 DC 1/12/2024 5:48:14 PM
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