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Missouri General Assembly· HB 264104/23/2026 - Delivered to Secretary of State (G)

Creates provisions relating to cannabis, the official text

Shown verbatim: the complete text as captured from the official PDF posted by the Missouri General Assembly, fetched 2026-09-25. Page and line markers are part of the official record; nothing is edited or removed. The official bill page.
SECOND REGULAR SESSION
                  [TRULY AGREED TO AND FINALLY PASSED]

                               SENATE SUBSTITUTE FOR
                      HOUSE COMMITTEE SUBSTITUTE FOR

               HOUSE BILL NO. 2641

               103RD GENERAL ASSEMBLY

    6366S.11T  2026

                                           AN ACT

    To repeal section 195.010, RSMo, and to enact in lieu thereof five new sections relating to
             cannabis, with penalty provisions and an effective date.

    Be it enacted by the General Assembly of the state of Missouri, as follows:

               Section A. Section 195.010, RSMo, is repealed and five new sections enacted in lieu

2 thereof, to be known as sections 195.010, 195.800, 195.819, 195.900, and 1, to read as

3 follows:

               195.010. The following words and phrases as used in this chapter and chapter 579,

2 unless the context otherwise requires, mean:

3              (1) "Acute pain", pain, whether resulting from disease, accidental or intentional

4 trauma, or other causes, that the practitioner reasonably expects to last only a short period of

5 time. Acute pain shall not include chronic pain, pain being treated as part of cancer care,

6 hospice or other end-of-life care, or medication-assisted treatment for substance use

7 disorders;

8              (2) "Addict", a person who habitually uses one or more controlled substances to such

9 an extent as to create a tolerance for such drugs, and who does not have a medical need for

10 such drugs, or who is so far addicted to the use of such drugs as to have lost the power of self-

11 control with reference to his or her addiction;

12             (3) "Administer", to apply a controlled substance, whether by injection, inhalation,

13 ingestion, or any other means, directly to the body of a patient or research subject by:

14             (a) A practitioner (or, in his or her presence, by his or her authorized agent); or

    EXPLANATION — Matter enclosed in bold-faced brackets [thus] in the above bill is not enacted and is
    intended to be omitted from the law. Matter in bold-face type in the above bill is proposed language.
SS HCS HB 2641                                  2

15       (b) The patient or research subject at the direction and in the presence of the

16 practitioner;

17       (4) "Agent", an authorized person who acts on behalf of or at the direction of a

18 manufacturer, distributor, or dispenser. The term does not include a common or contract

19 carrier, public warehouseman, or employee of the carrier or warehouseman while acting in the

20 usual and lawful course of the carrier's or warehouseman's business;

21       (5) "Attorney for the state", any prosecuting attorney, circuit attorney, or attorney

22 general authorized to investigate, commence and prosecute an action under this chapter;

23       (6) "Controlled substance", a drug, substance, or immediate precursor in Schedules I

24 through V listed in this chapter;

25       (7) "Controlled substance analogue", a substance the chemical structure of which is

26 substantially similar to the chemical structure of a controlled substance in Schedule I or II

27 and:

28       (a) Which has a stimulant, depressant, or hallucinogenic effect on the central nervous

29 system substantially similar to the stimulant, depressant, or hallucinogenic effect on the

30 central nervous system of a controlled substance included in Schedule I or II; or

31       (b) With respect to a particular individual, which that individual represents or intends

32 to have a stimulant, depressant, or hallucinogenic effect on the central nervous system

33 substantially similar to the stimulant, depressant, or hallucinogenic effect on the central

34 nervous system of a controlled substance included in Schedule I or II. The term does not

35 include a controlled substance; any substance for which there is an approved new drug

36 application; any substance for which an exemption is in effect for investigational use, for a

37 particular person, under Section 505 of the federal Food, Drug and Cosmetic Act (21 U.S.C.

38 Section 355) to the extent conduct with respect to the substance is pursuant to the exemption;

39 or any substance to the extent not intended for human consumption before such an exemption

40 takes effect with respect to the substance;

41       (8) "Counterfeit substance", a controlled substance which, or the container or labeling

42 of which, without authorization, bears the trademark, trade name, or other identifying mark,

43 imprint, number or device, or any likeness thereof, of a manufacturer, distributor, or dispenser

44 other than the person who in fact manufactured, distributed, or dispensed the substance;

45       (9) "Deliver" or "delivery", the actual, constructive, or attempted transfer from one

46 person to another of drug paraphernalia or of a controlled substance, or an imitation

47 controlled substance, whether or not there is an agency relationship, and includes a sale;

48       (10) "Dentist", a person authorized by law to practice dentistry in this state;

49       (11) "Depressant or stimulant substance":
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50  (a) A drug containing any quantity of barbituric acid or any of the salts of barbituric

51 acid or any derivative of barbituric acid which has been designated by the United States

52 Secretary of Health and Human Services as habit forming under 21 U.S.C. Section 352(d);

53  (b) A drug containing any quantity of:

54  a. Amphetamine or any of its isomers;

55  b. Any salt of amphetamine or any salt of an isomer of amphetamine; or

56  c. Any substance the United States Attorney General, after investigation, has found to

57 be, and by regulation designated as, habit forming because of its stimulant effect on the

58 central nervous system;

59  (c) Lysergic acid diethylamide; or

60  (d) Any drug containing any quantity of a substance that the United States Attorney

61 General, after investigation, has found to have, and by regulation designated as having, a

62 potential for abuse because of its depressant or stimulant effect on the central nervous system

63 or its hallucinogenic effect;

64  (12) "Dispense", to deliver a narcotic or controlled dangerous drug to an ultimate user

65 or research subject by or pursuant to the lawful order of a practitioner including the

66 prescribing, administering, packaging, labeling, or compounding necessary to prepare the

67 substance for such delivery. "Dispenser" means a practitioner who dispenses;

68  (13) "Distribute", to deliver other than by administering or dispensing a controlled

69 substance;

70  (14) "Distributor", a person who distributes;

71  (15) "Drug":

72  (a) Substances recognized as drugs in the official United States Pharmacopoeia,

73 Official Homeopathic Pharmacopoeia of the United States, or Official National Formulary, or

74 any supplement to any of them;

75  (b) Substances intended for use in the diagnosis, cure, mitigation, treatment or

76 prevention of disease in humans or animals;

77  (c) Substances, other than food, intended to affect the structure or any function of the

78 body of humans or animals; and

79  (d) Substances intended for use as a component of any article specified in this

80 subdivision. It does not include devices or their components, parts or accessories;

81  (16) "Drug-dependent person", a person who is using a controlled substance and who

82 is in a state of psychic or physical dependence, or both, arising from the use of such substance

83 on a continuous basis. Drug dependence is characterized by behavioral and other responses

84 which include a strong compulsion to take the substance on a continuous basis in order to

85 experience its psychic effects or to avoid the discomfort caused by its absence;
SS HCS HB 2641                       4

86   (17) "Drug enforcement agency", the Drug Enforcement Administration in the United

87 States Department of Justice, or its successor agency;

88   (18) "Drug paraphernalia", all equipment, products, substances and materials of any

89 kind which are used, intended for use, or designed for use, in planting, propagating,

90 cultivating, growing, harvesting, manufacturing, compounding, converting, producing,

91 processing, preparing, storing, containing, concealing, injecting, ingesting, inhaling, or

92 otherwise introducing into the human body a controlled substance or an imitation controlled

93 substance in violation of this chapter or chapter 579. It includes, but is not limited to:

94   (a) Kits used, intended for use, or designed for use in planting, propagating,

95 cultivating, growing or harvesting of any species of plant which is a controlled substance or

96 from which a controlled substance can be derived;

97   (b) Kits used, intended for use, or designed for use in manufacturing, compounding,

98 converting, producing, processing, or preparing controlled substances or imitation controlled

99 substances;

100  (c) Isomerization devices used, intended for use, or designed for use in increasing the

101 potency of any species of plant which is a controlled substance or an imitation controlled

102 substance;

103  (d) Testing equipment used, intended for use, or designed for use in identifying, or in

104 analyzing the strength, effectiveness or purity of controlled substances or imitation controlled

105 substances;

106  (e) Scales and balances used, intended for use, or designed for use in weighing or

107 measuring controlled substances or imitation controlled substances;

108  (f) Dilutents and adulterants, such as quinine hydrochloride, mannitol, mannite,

109 dextrose and lactose, used, intended for use, or designed for use in cutting controlled

110 substances or imitation controlled substances;

111  (g) Separation gins and sifters used, intended for use, or designed for use in removing

112 twigs and seeds from, or in otherwise cleaning or refining, marijuana;

113  (h) Blenders, bowls, containers, spoons and mixing devices used, intended for use, or

114 designed for use in compounding controlled substances or imitation controlled substances;

115  (i) Capsules, balloons, envelopes and other containers used, intended for use, or

116 designed for use in packaging small quantities of controlled substances or imitation controlled

117 substances;

118  (j) Containers and other objects used, intended for use, or designed for use in storing

119 or concealing controlled substances or imitation controlled substances;

120  (k) Hypodermic syringes, needles and other objects used, intended for use, or

121 designed for use in parenterally injecting controlled substances or imitation controlled

122 substances into the human body;
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123      (l) Objects used, intended for use, or designed for use in ingesting, inhaling, or

124 otherwise introducing marijuana, cocaine, hashish, or hashish oil into the human body, such

125 as:

126      a. Metal, wooden, acrylic, glass, stone, plastic, or ceramic pipes with or without

127 screens, permanent screens, hashish heads, or punctured metal bowls;

128      b. Water pipes;

129      c. Carburetion tubes and devices;

130      d. Smoking and carburetion masks;

131      e. Roach clips meaning objects used to hold burning material, such as a marijuana

132 cigarette, that has become too small or too short to be held in the hand;

133      f. Miniature cocaine spoons and cocaine vials;

134      g. Chamber pipes;

135      h. Carburetor pipes;

136      i. Electric pipes;

137      j. Air-driven pipes;

138      k. Chillums;

139      l. Bongs;

140      m. Ice pipes or chillers;

141      (m) Substances used, intended for use, or designed for use in the manufacture of a

142 controlled substance.

143

144 In determining whether an object, product, substance or material is drug paraphernalia, a

145 court or other authority should consider, in addition to all other logically relevant factors, the

146 following:

147      a. Statements by an owner or by anyone in control of the object concerning its use;

148      b. Prior convictions, if any, of an owner, or of anyone in control of the object, under

149 any state or federal law relating to any controlled substance or imitation controlled substance;

150      c. The proximity of the object, in time and space, to a direct violation of this chapter

151 or chapter 579;

152      d. The proximity of the object to controlled substances or imitation controlled

153 substances;

154      e. The existence of any residue of controlled substances or imitation controlled

155 substances on the object;

156      f. Direct or circumstantial evidence of the intent of an owner, or of anyone in control

157 of the object, to deliver it to persons who he or she knows, or should reasonably know, intend

158 to use the object to facilitate a violation of this chapter or chapter 579; the innocence of an

159 owner, or of anyone in control of the object, as to direct violation of this chapter or chapter
SS HCS HB 2641                                    6

160 579 shall not prevent a finding that the object is intended for use, or designed for use as drug

161 paraphernalia;

162  g. Instructions, oral or written, provided with the object concerning its use;

163  h. Descriptive materials accompanying the object which explain or depict its use;

164  i. National or local advertising concerning its use;

165  j. The manner in which the object is displayed for sale;

166  k. Whether the owner, or anyone in control of the object, is a legitimate supplier of

167 like or related items to the community, such as a licensed distributor or dealer of tobacco

168 products;

169  l. Direct or circumstantial evidence of the ratio of sales of the object to the total sales

170 of the business enterprise;

171  m. The existence and scope of legitimate uses for the object in the community;

172  n. Expert testimony concerning its use;

173  o. The quantity, form or packaging of the product, substance or material in relation to

174 the quantity, form or packaging associated with any legitimate use for the product, substance

175 or material;

176  (19) "Federal narcotic laws", the laws of the United States relating to controlled

177 substances;

178  (20) "Hemp", the same meaning given to the term in section 195.900;

179  (21) "Hospital", a place devoted primarily to the maintenance and operation of

180 facilities for the diagnosis, treatment or care, for not less than twenty-four hours in any week,

181 of three or more nonrelated individuals suffering from illness, disease, injury, deformity or

182 other abnormal physical conditions; or a place devoted primarily to provide, for not less than

183 twenty-four consecutive hours in any week, medical or nursing care for three or more

184 nonrelated individuals. The term hospital does not include convalescent, nursing, shelter or

185 boarding homes as defined in chapter 198;

186  [(21) "Illegal industrial hemp":

187  [(a) All nonseed parts and varieties of the Cannabis sativa L. plant, growing or not,

188 that contain an average delta-9 tetrahydrocannabinol (THC) concentration exceeding three-

189 tenths of one percent on a dry weight basis;

190  [(b) Illegal industrial hemp shall be destroyed in the most effective manner possible,

191 and such destruction shall be verified by the Missouri state highway patrol;]

192  (22) "Immediate precursor", a substance which:

193  (a) The state department of health and senior services has found to be and by rule

194 designates as being the principal compound commonly used or produced primarily for use in

195 the manufacture of a controlled substance;
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196  (b) Is an immediate chemical intermediary used or likely to be used in the

197 manufacture of a controlled substance; and

198  (c) The control of which is necessary to prevent, curtail or limit the manufacture of

199 the controlled substance;

200  (23) "Imitation controlled substance", a substance that is not a controlled substance,

201 which by dosage unit appearance (including color, shape, size and markings), or by

202 representations made, would lead a reasonable person to believe that the substance is a

203 controlled substance. In determining whether the substance is an imitation controlled

204 substance the court or authority concerned should consider, in addition to all other logically

205 relevant factors, the following:

206  (a) Whether the substance was approved by the federal Food and Drug

207 Administration for over-the-counter (nonprescription or nonlegend) sales and was sold in

208 the federal Food and Drug Administration-approved package, with the federal Food and Drug

209 Administration-approved labeling information;

210  (b) Statements made by an owner or by anyone else in control of the substance

211 concerning the nature of the substance, or its use or effect;

212  (c) Whether the substance is packaged in a manner normally used for illicit controlled

213 substances;

214  (d) Prior convictions, if any, of an owner, or anyone in control of the object, under

215 state or federal law related to controlled substances or fraud;

216  (e) The proximity of the substances to controlled substances;

217  (f) Whether the consideration tendered in exchange for the noncontrolled substance

218 substantially exceeds the reasonable value of the substance considering the actual chemical

219 composition of the substance and, where applicable, the price at which over-the-counter

220 substances of like chemical composition sell. An imitation controlled substance does not

221 include a placebo or registered investigational drug either of which was manufactured,

222 distributed, possessed or delivered in the ordinary course of professional practice or research;

223  (24) "Industrial hemp"[:

224  (a) All nonseed parts and varieties of the Cannabis sativa L. plant, growing or not,

225 that contain an average delta-9 tetrahydrocannabinol (THC) concentration that does not

226 exceed three-tenths of one percent on a dry weight basis or the maximum concentration

227 allowed under federal law, whichever is greater;

228  (b) Any Cannabis sativa L. seed that is part of a growing crop, retained by a grower

229 for future planting, or used for processing into or use as agricultural hemp seed;

230  (c) Industrial hemp includes industrial hemp commodities and products and topical or

231 ingestible animal and consumer products derived from industrial hemp with a delta-9
SS HCS HB 2641                                 8

232 tetrahydrocannabinol concentration of not more than three-tenths of one percent on a dry

233 weight basis], the same meaning given to the term in section 195.900;

234  (25) "Initial prescription", a prescription issued to a patient who has never previously

235 been issued a prescription for the drug or its pharmaceutical equivalent or who was previously

236 issued a prescription for the drug or its pharmaceutical equivalent, but the date on which the

237 current prescription is being issued is more than five months after the date the patient last

238 used or was administered the drug or its equivalent;

239  (26) "Laboratory", a laboratory approved by the department of health and senior

240 services as proper to be entrusted with the custody of controlled substances but does not

241 include a pharmacist who compounds controlled substances to be sold or dispensed on

242 prescriptions;

243  (27) "Manufacture", the production, preparation, propagation, compounding or

244 processing of drug paraphernalia or of a controlled substance, or an imitation controlled

245 substance, either directly or by extraction from substances of natural origin, or independently

246 by means of chemical synthesis, or by a combination of extraction and chemical synthesis,

247 and includes any packaging or repackaging of the substance or labeling or relabeling of its

248 container. This term does not include the preparation or compounding of a controlled

249 substance or an imitation controlled substance or the preparation, compounding, packaging or

250 labeling of a narcotic or dangerous drug:

251  (a) By a practitioner as an incident to his or her administering or dispensing of a

252 controlled substance or an imitation controlled substance in the course of his or her

253 professional practice; or

254  (b) By a practitioner or his or her authorized agent under his or her supervision, for

255 the purpose of, or as an incident to, research, teaching or chemical analysis and not for sale;

256  (28) "Marijuana", all parts of the plant genus Cannabis in any species or form thereof,

257 including, but not limited to Cannabis Sativa L., except industrial hemp, Cannabis Indica,

258 Cannabis Americana, Cannabis Ruderalis, and Cannabis Gigantea, whether growing or not,

259 the seeds thereof, the resin extracted from any part of the plant; and every compound,

260 manufacture, salt, derivative, mixture, or preparation of the plant, its seeds or resin. It does

261 not include the mature stalks of the plant, fiber produced from the stalks, oil or cake made

262 from the seeds of the plant, any other compound, manufacture, salt, derivative, mixture or

263 preparation of the mature stalks (except the resin extracted therefrom), fiber, oil or cake, or

264 the sterilized seed of the plant which is incapable of germination;

265  (29) "Methamphetamine precursor drug", any drug containing ephedrine,

266 pseudoephedrine, phenylpropanolamine, or any of their salts, optical isomers, or salts of

267 optical isomers;
SS HCS HB 2641                                 9

268         (30) "Narcotic drug", any of the following, whether produced directly or indirectly by

269 extraction from substances of vegetable origin, or independently by means of chemical

270 synthesis, or by a combination of extraction and chemical analysis:

271         (a) Opium, opiate, and any derivative, of opium or opiate, including their isomers,

272 esters, ethers, salts, and salts of isomers, esters, and ethers, whenever the existence of the

273 isomers, esters, ethers, and salts is possible within the specific chemical designation. The

274 term does not include the isoquinoline alkaloids of opium;

275         (b) Coca leaves, but not including extracts of coca leaves from which cocaine,

276 ecgonine, and derivatives of ecgonine or their salts have been removed;

277         (c) Cocaine or any salt, isomer, or salt of isomer thereof;

278         (d) Ecgonine, or any derivative, salt, isomer, or salt of isomer thereof;

279         (e) Any compound, mixture, or preparation containing any quantity of any substance

280 referred to in paragraphs (a) to (d) of this subdivision;

281         (31) "Official written order", an order written on a form provided for that purpose by

282 the United States Commissioner of Narcotics, under any laws of the United States making

283 provision therefor, if such order forms are authorized and required by federal law, and if no

284 such order form is provided, then on an official form provided for that purpose by the

285 department of health and senior services;

286         (32) "Opiate" or "opioid", any substance having an addiction-forming or addiction-

287 sustaining liability similar to morphine or being capable of conversion into a drug having

288 addiction-forming or addiction-sustaining liability. The term includes its racemic and

289 levorotatory forms. It does not include, unless specifically controlled under section 195.017,

290 the dextrorotatory isomer of 3-methoxy-n-methyl-morphinan and its salts

291 (dextromethorphan);

292         (33) "Opium poppy", the plant of the species Papaver somniferum L., except its

293 seeds;

294         (34) "Over-the-counter sale", a retail sale licensed pursuant to chapter 144 of a drug

295 other than a controlled substance;

296         (35) "Person", an individual, corporation, government or governmental subdivision or

297 agency, business trust, estate, trust, partnership, joint venture, association, or any other legal

298 or commercial entity;

299         (36) "Pharmacist", a licensed pharmacist as defined by the laws of this state, and

300 where the context so requires, the owner of a store or other place of business where controlled

301 substances are compounded or dispensed by a licensed pharmacist; but nothing in this chapter

302 shall be construed as conferring on a person who is not registered nor licensed as a pharmacist

303 any authority, right or privilege that is not granted to him by the pharmacy laws of this state;

304         (37) "Poppy straw", all parts, except the seeds, of the opium poppy, after mowing;
SS HCS HB 2641                                  10

305         (38) "Possessed" or "possessing a controlled substance", a person, with the

306 knowledge of the presence and nature of a substance, has actual or constructive possession of

307 the substance. A person has actual possession if he has the substance on his or her person or

308 within easy reach and convenient control. A person who, although not in actual possession,

309 has the power and the intention at a given time to exercise dominion or control over the

310 substance either directly or through another person or persons is in constructive possession of

311 it. Possession may also be sole or joint. If one person alone has possession of a substance

312 possession is sole. If two or more persons share possession of a substance, possession is

313 joint;

314         (39) "Practitioner", a physician, dentist, optometrist, podiatrist, veterinarian, scientific

315 investigator, pharmacy, hospital or other person licensed, registered or otherwise permitted by

316 this state to distribute, dispense, conduct research with respect to or administer or to use in

317 teaching or chemical analysis, a controlled substance in the course of professional practice or

318 research in this state, or a pharmacy, hospital or other institution licensed, registered, or

319 otherwise permitted to distribute, dispense, conduct research with respect to or administer a

320 controlled substance in the course of professional practice or research;

321         (40) "Production", includes the manufacture, planting, cultivation, growing, or

322 harvesting of drug paraphernalia or of a controlled substance or an imitation controlled

323 substance;

324         (41) "Registry number", the number assigned to each person registered under the

325 federal controlled substances laws;

326         (42) "Sale", includes barter, exchange, or gift, or offer therefor, and each such

327 transaction made by any person, whether as principal, proprietor, agent, servant or employee;

328         (43) "State" when applied to a part of the United States, includes any state, district,

329 commonwealth, territory, insular possession thereof, and any area subject to the legal

330 authority of the United States of America;

331         (44) "Synthetic cannabinoid", includes unless specifically excepted or unless listed in

332 another schedule, any natural or synthetic material, compound, mixture, or preparation that

333 contains any quantity of a substance that is a cannabinoid receptor agonist, including but not

334 limited to any substance listed in paragraph (ll) of subdivision (4) of subsection 2 of section

335 195.017 and any analogues; homologues; isomers, whether optical, positional, or geometric;

336 esters; ethers; salts; and salts of isomers, esters, and ethers, whenever the existence of the

337 isomers, esters, ethers, or salts is possible within the specific chemical designation, however,

338 it shall not include any approved pharmaceutical authorized by the United States Food and

339 Drug Administration;

340         (45) "Ultimate user", a person who lawfully possesses a controlled substance or an

341 imitation controlled substance for his or her own use or for the use of a member of his or her
SS HCS HB 2641                                 11

342 household or immediate family, regardless of whether they live in the same household, or for

343 administering to an animal owned by him or by a member of his or her household. For

344 purposes of this section, the phrase "immediate family" means a husband, wife, parent, child,

345 sibling, stepparent, stepchild, stepbrother, stepsister, grandparent, or grandchild;

346  (46) "Wholesaler", a person who supplies drug paraphernalia or controlled substances

347 or imitation controlled substances that he himself has not produced or prepared, on official

348 written orders, but not on prescriptions.

     195.800. 1. Notwithstanding any other provision of law to the contrary, no state

2 agency, including employees therein, shall disclose to the federal government, any

3 federal government employee, or any unauthorized third party the statewide list or any

4 individual information of persons who have applied for or obtained a qualifying patient

5 identification card, a qualifying patient cultivation identification card, or a primary

6 caregiver identification card, as those cards are described in Article XIV, Section 1 of

7 the Constitution of Missouri relating to the right to access medical marijuana, unless

8 required to do so pursuant to a subpoena or court order issued by a court of competent

9 jurisdiction.

10   2. Any person who knowingly violates the provisions of this section shall be

11 guilty of a class E felony.

     195.819. Marijuana dispensary facilities, as described in Article XIV of the

2 Constitution of Missouri, shall not create or retain any record containing the

3 consumer's identifying information; provided, that a facility may create or retain

4 such records if the consumer affirmatively agrees to such, in writing, and if the facility

5 does not refuse to provide services or sell goods to the consumer if he or she does not

6 agree to the creation or retention of such records. The provisions of this section shall

7 not apply to any record-keeping requirements relating to qualifying patients and

8 primary caregivers under Article XIV, Section 1 of the Constitution of Missouri. Any

9 dispensary facility that violates the provisions of this section shall be assessed a five-

10 hundred-dollar fine per occurrence.

     195.900. 1. This section shall be known and may be cited as the "Intoxicating

2 Cannabinoid Control Act".

3    2. As used in this section, the following terms mean:

4    (1) "Department", the department of health and senior services;

5    (2) "Division", the division of alcohol and tobacco control within the department

6 of public safety;

7    (3) "Hemp", the plant Cannabis sativa L. and any part of that plant, including

8 the seeds thereof, and all derivatives, extracts, cannabinoids, isomers, acids, salts, and

9 salts of isomers, whether growing or not, with a total tetrahydrocannabinol
SS HCS HB 2641                 12

10 concentration, including tetrahydrocannabinolic acid, of not more than three-tenths of

11 one percent on a dry-weight basis. "Hemp" shall include industrial hemp but shall not

12 include the following:

13  (a) Any viable seed from a Cannabis sativa L. plant that exceeds a total

14 tetrahydrocannabinol concentration, including tetrahydrocannabinolic acid, of three-

15 tenths of one percent on a dry-weight basis;

16  (b) Any intermediate hemp-derived cannabinoid products containing:

17  a. Cannabinoids that are not capable of being naturally produced by a Cannabis

18 sativa L. plant;

19  b. Cannabinoids that are capable of being naturally produced by a Cannabis

20 sativa L. plant but that were synthesized or manufactured outside the plant; or

21  c. More than three-tenths of one percent on a dry-weight basis of a combined

22 total of tetrahydrocannabinols, including tetrahydrocannabinolic acid, and any other

23 cannabinoids that have similar effects or are marketed as having similar effects on

24 humans or animals as a tetrahydrocannabinol, as determined by the U.S. Secretary of

25 Health and Human Services;

26  (c) Any intermediate hemp-derived cannabinoid products marketed or sold as a

27 final product or directly to an end consumer for personal or household use; or

28  (d) Any final hemp-derived cannabinoid products containing:

29  a. Cannabinoids that are not capable of being naturally produced by a Cannabis

30 sativa L. plant;

31  b. Cannabinoids that are capable of being naturally produced by a Cannabis

32 sativa L. plant but that were synthesized or manufactured outside the plant; or

33  c. Greater than four-tenths of one milligram combined total per container of

34 tetrahydrocannabinols, including tetrahydrocannabinolic acid, and any other

35 cannabinoids that have similar effects or are marketed as having similar effects on

36 humans or animals as a tetrahydrocannabinol, as determined by the U.S. Secretary of

37 Health and Human Services;

38  (4) "Hemp-derived cannabinoid product", any intermediate or final product

39 derived from hemp, other than industrial hemp, that contains cannabinoids in any form

40 and is intended for human or animal use through any means of application or

41 administration including, but not limited to, inhalation, ingestion, or topical application.

42 "Hemp-derived cannabinoid product" shall not include a drug that is the subject of an

43 application approved under subsection (c) or (j) of Section 505 of the Federal Food,

44 Drug, and Cosmetic Act, 21 U.S.C. Section 355, as amended;

45  (5) "Industrial hemp", hemp that is:
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46  (a) Grown for the use of the stalk of the plant, fiber produced from such a stalk,

47 or any other noncannabinoid compound, derivative, mixture, preparation, or

48 manufacture of such a stalk;

49  (b) Grown for the use of the whole grain, oil, cake, nut, hull, or any other

50 noncannabinoid compound, derivative, mixture, preparation, or manufacture of the

51 seeds of such plant;

52  (c) Grown for the purpose of producing microgreens or other edible hemp leaf

53 products intended for human consumption that are derived from an immature hemp

54 plant that is grown from seeds that do not exceed the threshold for total

55 tetrahydrocannabinol concentration under paragraph (a) of subdivision (3) of this

56 subsection;

57  (d) A plant that does not enter the stream of commerce and is intended to

58 support hemp research at an institution of higher education, as defined in Section 101 of

59 the Higher Education Act of 1965, 20 U.S.C. Section 1001, as amended, or an

60 independent research institute; or

61  (e) Grown for the use of a viable seed of the plant produced solely for the

62 production or manufacture of any material described in paragraphs (a) to (d) of this

63 subdivision;

64  (6) "Intermediate hemp-derived cannabinoid product", a hemp-derived

65 cannabinoid product that is:

66  (a) Not yet in the final form or preparation marketed or intended to be used or

67 consumed by a human or animal; or

68  (b) A powder, liquid, tablet, oil, or other product form that is intended or

69 marketed to be mixed, dissolved, formulated, or otherwise added to or prepared with or

70 into any other substance prior to administration or consumption;

71  (7) "Marijuana", the same meaning given to the term in Article XIV of the

72 Constitution of Missouri. The term "marijuana" shall not be construed to conform to

73 or be included in the definition of "hemp" in this section;

74  (8) "Transaction", the sale of a single unit of a hemp-derived cannabinoid

75 product, including a single unit in a multiunit package.

76  3. The cultivation, production, manufacturing, testing, transportation, and retail

77 sale of all hemp-derived cannabinoid products within this state shall be conducted solely

78 by entities licensed by the department under Article XIV of the Constitution of

79 Missouri. Hemp-derived cannabinoid products shall be considered marijuana and shall

80 be subject to the legal framework contained in Article XIV of the Constitution of

81 Missouri under which the purchase, possession, consumption, use, delivery,

82 manufacturing, and sale of marijuana is regulated by the department.
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83   4. The term "hemp-derived cannabinoid product" shall be construed to conform

84 to, and be included in, the definition of "marijuana" under Article XIV of the

85 Constitution of Missouri but shall not be construed to conform to or be included in the

86 definition of "hemp" in this section or in the definition of "industrial hemp" in this

87 section.

88   5. Hemp and industrial hemp shall not be considered marijuana and shall not be

89 subject to the legal framework contained in Article XIV of the Constitution of Missouri

90 or in this section. Nothing in this section shall be construed to regulate hemp, industrial

91 hemp, or products that do not fall within the definition of hemp-derived cannabinoid

92 products, and the provisions of this section shall not be construed to conflict with or

93 otherwise preempt the Agriculture Improvement Act of 2018, Pub. L. 115-334, as

94 amended.

95   6. Nothing in this section shall be construed to prohibit the interstate commerce

96 of hemp or the transportation or shipment of hemp through this state.

97   7. Notwithstanding any provision of law to the contrary, all hemp-derived

98 cannabinoid products are marijuana and shall be subject to the jurisdiction of the

99 department and the office of the attorney general consistent with Article XIV of the

100 Constitution of Missouri and the provisions of this section. The department and the

101 office of the attorney general shall be authorized to enforce the provisions of this section

102 in such a manner as to ensure that no hemp-derived cannabinoid products are

103 cultivated, manufactured, tested, transported, or sold within this state outside of a

104 licensed comprehensive facility, medical facility, marijuana testing facility, or marijuana

105 microbusiness facility, as such terms are defined in Article XIV of the Constitution of

106 Missouri.

107  8. No person or entity engaged in the sale of products that contain cannabidiol,

108 hemp, marijuana, or cannabinoids; hemp-derived cannabinoid products; or

109 paraphernalia to aid in the human or animal consumption of such products, other

110 than a comprehensive marijuana dispensary facility, medical marijuana dispensary

111 facility, or microbusiness dispensary facility, as such terms are defined in Article XIV of

112 the Constitution of Missouri, shall carry on, conduct, or transact business under a name

113 that contains as part of the name the word "dispensary" or any word of similar import.

114  9. (1) The office of the attorney general, the department, the department of

115 public safety, the division, the Missouri state highway patrol, and any other state agency

116 deemed necessary by the office of the attorney general to aid in the enforcement of this

117 section shall concurrently be authorized to enforce the provisions of this section

118 including, but not limited to, the prohibition of the cultivation, manufacturing, testing,

119 transportation, and retail sale of hemp-derived cannabinoid products outside of licensed
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120 comprehensive facilities, medical facilities, marijuana testing facilities, or marijuana

121 microbusiness facilities, as such terms are defined in Article XIV of the Constitution of

122 Missouri.

123          (2) The office of the attorney general shall have primary jurisdiction to enforce

124 the provisions of this section including, but not limited to:

125          (a) Utilizing a multijurisdictional enforcement approach including, but not

126 limited to, direct coordination with the department, the department of public safety, the

127 division, the Missouri state highway patrol, prosecuting and circuit attorneys, and any

128 other state agency deemed necessary by the office of the attorney general;

129          (b) Collaborating and coordinating with local county and municipal

130 governments and other political subdivisions; and

131          (c) Utilizing the department's reference laboratory.

132          10. Any person or entity that violates the provisions of this section shall be

133 subject to a fine of five thousand dollars per transaction and shall be guilty of a class D

134 felony.

135          11. (1) The provisions of this section shall become effective November 12, 2026,

136 for:

137          (a) Hemp-derived cannabinoid products that:

138          a. Contain cannabinoids that are not capable of being naturally produced by a

139 Cannabis sativa L. plant;

140          b. Contain cannabinoids that are capable of being naturally produced by a

141 Cannabis sativa L. plant but that were synthesized or manufactured outside the plant;

142          c. Are sold, distributed, or marketed to a consumer as a product that can be

143 smokable or vapeable in the form of raw plant material, flower, or bud material and

144 that contain any amount of tetrahydrocannabinolic acid; or

145          d. Are sold, distributed, or marketed to a consumer in the form of any solid

146 candy, gummy, chewable product, tablet, capsule, oil, baked good, or other solid edible

147 product and that contain delta-9 tetrahydrocannabinol derived from hemp in any

148 amount that exceeds naturally occurring concentrations in the source hemp plant

149 material; and

150          (b) Except as provided in subdivision (2) of this subsection, all other hemp-

151 derived cannabinoid products not described in paragraph (a) of this subdivision.

152          (2) For all other hemp-derived cannabinoid products not described in

153 paragraph (a) of subdivision (1) of this subsection, the provisions of this section shall

154 become effective November 12, 2026, except that if Congress delays the effective date of

155 federal hemp restrictions under 7 U.S.C. Section 1639o on or before November 12, 2026,

156 this section shall apply to such products only during any period in which such federal
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157 restrictions prohibit such products; provided, that such products shall not be sold,
158 distributed, or marketed to any person under the age of twenty-one.

                Section 1. All persons employed in cannabis-related businesses in this state,
   2 including cultivation, processing, manufacturing, distribution, retail, and support
   3 operations, shall have the right to organize, form, join, and assist labor organizations
   4 and to bargain collectively with their employers through representatives of their own
   5 choosing. Cannabis industry employment, including work in climate-controlled indoor
   6 cultivation and processing facilities, is not "agricultural labor" as used for purposes of
   7 exemptions from collective bargaining and shall be treated as covered employment
   8 under Missouri's collective bargaining protections.

                Section B. The enactment of sections 195.800, 195.819 and 195.900 and the repeal
   2 and reenactment of section 195.010 shall become effective on November 12, 2026.

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