Oklahoma Code § 63-1-1432.4

Title 63. Public Health And Safety: Prohibited products – Labeling requirements –
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Distribution to minors prohibited – Test results.
A.  A vendor shall not prepare, distribute, sell, or expose for
sale any of the following:
1.  A kratom product that does not meet the definition for a
kratom product pursuant to Section 1-1432.2 of this title;
2.  A kratom product that is contaminated with a dangerous
nonkratom substance.  A kratom product is contaminated with a
dangerous nonkratom substance if the kratom product contains a
substance that is not safe for human consumption;
3.  A kratom product containing a level of 7-hydroxymitragynine
in the alkaloid fraction that is greater than one percent (1%) of
the alkaloid composition of the product;
4.  A kratom product containing any synthesized alkaloid
including synthesized mitragynine, synthesized 7-hydroxymitragynine
or any other synthesized compounds of the kratom plant;
5.  A kratom product containing any controlled substance listed
in the Uniform Controlled Dangerous Substances Act, unless the
product is compounded by a licensed pharmacist with the controlled
substance dispensed in accordance with a valid prescription; or
6.  A kratom product containing a level of any residual solvent
that was used in the manufacturing of the extract that exceeds the
residual level specified for pharmaceutical products in the document
“Q3C - Tables and List, Guidance for Industry, (June 2017) ICH
Revision 3” issued by the United States Department of Health and
Human Services, Food and Drug Administration.
B.  Kratom products shall be accompanied by a label 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 prohibited;
3.  The amount of total kratom alkaloids, mitragynine, and 7-
hydroxymitragynine contained in the product;
4.  The amount of total kratom alkaloids, mitragynine, 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 distributing the product;
6.  Any federal food allergen labeling requirements, if
applicable, and clear and adequate directions for the consumption
and safe and effective use of such product, including the
recommended serving size, the number of servings in the container,
and the number of servings that can be safely consumed in a day.
Provided, liquid kratom products shall be packaged in a retail

container that has clear serving size markings and be subject to the
following requirements:
a. products of less than eight (8) fluid ounces which
contain more than three servings shall be accompanied
by a calibrated measuring device, and
b. if such a product contains more than the eight (8)
fluid ounces, the requirements specified in
subparagraph a of this paragraph do not apply;
7.  Any precautionary statements as to the safety and
effectiveness of the product, including a warning that a consumer
should consult a health care professional on questions about the use
of kratom and that the product may be habit-forming; and
8.  A statement that states, “These statements have not been
evaluated by the United States Food and Drug Administration.  This
product is not intended to diagnose, treat, cure, or prevent any
disease.”
C.  A vendor may not distribute, sell, or expose for sale a
kratom product to an individual under eighteen (18) years of age.
D.  Upon request by the State Department of Health, the vendor
shall provide test results from a United States-based testing
facility, that is an independent testing laboratory as defined in
Section 1-1432.2 of this title, to confirm the items listed on the
product label.
Added by Laws 2021, c. 500, § 4, eff. Nov. 1, 2021.  Amended by Laws
2024, c. 278, § 2, eff. Nov. 1, 2024; Laws 2025, c. 299, § 2, eff.
Nov. 1, 2025.

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