As of November 12, 2026, Kava (Piper methysticum) is legal to sell at retail with restrictions in Utah. Not scheduled; Utah alcohol law excludes products with kava as an alcohol-masking additive from beer and heavy beer. Controlling source: Utah Code 32B-1-102(12), (53) (beer and heavy beer definitions).
Verified November 12, 2026 (hash check) · confidence: confirmedIs Kava Legal? Every state and federal law
Kava is not on Utah's controlled-substance schedules: the Schedule I hallucinogenic list (Utah Code 58-37-108(2)(a)(iii), chapter effective July 1, 2026) does not name kava, Piper methysticum or kavalactones, and the Kratom Regulation Act (Title 4, Chapter 45) does not mention it. One statute names kava: the Alcoholic Beverage Control Act definitions, Utah Code 32B-1-102(12)(c)(iii) and (53)(c)(iii), provide that “beer” and "heavy beer" do not include a product that contains an additive masking or altering a physiological effect of alcohol, including kratom, kava, cannabidiol, or tetrahydrocannabinol (language added by H.B. 247, 2023 General Session). A kava-containing malt beverage therefore cannot be sold as beer (the category grocery and convenience beer retailers sell) or as heavy beer in Utah; how such a product is otherwise classified under Title 32B is not addressed in the text and is not resolved here. The rule reaches kava combined with alcohol only; non-alcoholic kava beverages, powders and supplements are outside it, so a lawful retail path remains and the provision is recorded as a kava-specific combination-product condition. H.B. 601 (2026), which would have added similar language to 32B-7-102, was not enacted. A full-text sweep of 345 Utah Code chapters found no other provision naming kava. Neither the plant nor its alkaloids are federally controlled; FDA food and supplement law applies (see the federal page).
(c) “Beer” does not include: (i) a flavored malt beverage; (ii) a product that contains alcohol derived from: (A) except as provided in Subsection (12)(b)(iii), spirituous liquor; or (B) wine; or (iii) a product that contains an additive masking or altering a physiological effect of alcohol, including kratom, kava, cannabidiol, or natural or synthetic tetrahydrocannabinol.
Among Utah's 6 neighbors, Arizona, Colorado, Idaho, Nevada, New Mexico and Wyoming are legal.
Open the interactive map · Every compound in Utah · Where Kava is banned · Kava shots and kava drinks by state · Kava and kratom drinks by state · Embed this map
Not federally scheduled. Not federally controlled; sold under FDA dietary supplement and food law Federal detail
12 instruments on file for this compound’s framework in Utah; 4 of 4 citations above are official sources. Each text carries its source and a fingerprint that changes when the law does.
a8989892fcbac0ca(iii) Unless specifically excepted or unless listed in another schedule, any material, compound, mixture, or preparation which contains any quantity of the following hallucinogenic substances, or which contains any of their salts, isomers, and salts of isomers when the existence of the salts, isomers, and salts of isomers is possible within the specific chemical designation; as used in this Subsection (2)(a)(iii) only, "isomer" includes the optical, position, and geometric isomers:
17d9296376636927(a) “Beer” means a product that: (i) contains: (A) at least .5% of alcohol by volume; and (B) no more than 5% of alcohol by volume or 4% by weight; (ii) is obtained by fermentation, infusion, or decoction of: (A) malt; or (B) a malt substitute; and (iii) is clearly marketed, labeled, and identified as: (A) beer; (B) ale; (C) porter; (D) stout; (E) lager; (F) a malt; (G) a malted beverage; or (H) seltzer. (b) “Beer” may contain: Page 2 Utah Code (i) hops extract; (ii) caffeine, if the caffeine is a natural constituent of an added ingredient; or (iii) a propylene glycol-, ethyl alcohol-, or ethanol-based flavoring agent that: (A) is used in the production of beer; (B) is in a formula approved by the federal Alcohol and Tobacco Tax and Trade Bureau after the formula is filed for approval under 27 C.F.R. Sec. 25.55; and (C) does not contribute more than 10% of the overall alcohol content of the beer. (c) “Beer” does not include: (i) a flavored malt beverage; (ii) a product that contains alcohol derived from: (A) except as provided in Subsection (12)(b)(iii), spirituous liquor; or (B) wine; or (iii) a product that contains an additive masking or altering a physiological effect of alcohol, including kratom, kava, cannabidiol, or natural or synthetic tetrahydrocannabinol. (a) "Heavy beer" means a product that: (i) (A) contains more than 5% alcohol by volume; Page 6 Utah Code (B) contains at least .5% of alcohol by volume and no more than 5% of alcohol by volume or 4% by weight, and a propolyne glycol-, ethyl alcohol-, or ethanol-based flavoring agent that contributes more than 10% of the overall alcohol content of the product; or (C) contains at least .5% of alcohol by volume and no more than 5% of alcohol by volume or 4% by weight, and has a label or packaging that is rejected under Subsection 32B-1-606(3)(b); and (ii) is obtained by fermentation, infusion, or decoction of: (A) malt; or (B) a malt substitute. (b) "Heavy beer" may, if the heavy beer contains more than 5% alcohol by volume, contain a propolyne glycol-, ethyl alcohol-, or ethanol-based flavoring agent that contributes to the overall alcohol content of the heavy beer. (c) "Heavy beer" does not include: (i) a flavored malt beverage; (ii) a product that contains alcohol derived from: (A) except as provided in Subsections (53)(a)(i)(B) and (53)(b), spirituous liquor; or (B) wine; or (iii) a product that contains an additive masking or altering a physiological effect of alcohol, including kratom, kava, cannabidiol, or natural or synthetic tetrahydrocannabinol. (d) "Heavy beer" is considered liquor for the purposes of this title.
41bf1e4ee4b34dca(e)
(i) “Controlled substance” means a drug or substance:
(A) included in Schedules I, II, III, IV, or V of Section 58-37-108;
(B) included in Schedules I, II, III, IV, or V of the federal Controlled Substances Act, Title II,
P.L. 91-513;
(C) that is a controlled substance analog; or
(D) listed in Section 58-37-109.
(ii) “Controlled substance” does not include:
(A) distilled spirits, wine, or malt beverages, as those terms are defined in Title 32B, Alcoholic
Beverage Control Act;
(B) any drug intended for lawful use in the diagnosis, cure, mitigation, treatment, or prevention
of disease in human or other animals, which contains ephedrine, pseudoephedrine,
norpseudoephedrine, or phenylpropanolamine if the drug is lawfully purchased, sold,
transferred, or furnished as an over-the-counter medication without prescription; or
(C) dietary supplements, vitamins, minerals, herbs, or other similar substances including
concentrates or extracts, which:
(I) are not otherwise regulated by law; and
(II) may contain naturally occurring amounts of chemicals or substances listed in this
chapter, or in rules made in accordance with Title 63G, Chapter 3, Utah Administrative
Rulemaking Act.
(f)
(i) “Controlled substance analog” means:
(A) a substance the chemical structure of which is substantially similar to the chemical
structure of a controlled substance listed in Schedules I and II of Section 58-37-108, a
substance listed in Section 58-37-109, or in Schedules I and II of the federal Controlled
Substances Act, Title II, P.L. 91-513;
(B) a substance that has a stimulant, depressant, or hallucinogenic effect on the central
nervous system substantially similar to the stimulant, depressant, or hallucinogenic
effect on the central nervous system of controlled substances listed in Schedules I and
II of Section 58-37-108, substances listed in Section 58-37-109, or substances listed in
Schedules I and II of the federal Controlled Substances Act, Title II, P.L. 91-513; or
(C) a substance that, with respect to a particular individual, is represented or intended to
have a stimulant, depressant, or hallucinogenic effect on the central nervous system
substantially similar to the stimulant, depressant, or hallucinogenic effect on the central
nervous system of controlled substances listed in Schedules I and II of Section 58-37-108,
substances listed in Section 58-37-109, or substances listed in Schedules I and II of the
federal Controlled Substances Act, Title II, P.L. 91-513.
(ii) “Controlled substance analog” does not include:
(A) a controlled substance currently scheduled in Schedules I through V of Section
58-37-108;
(B) a substance for which there is an approved new drug application;
(C) a substance with respect to which an exemption is in effect for investigational use by a
particular person under Section 505 of the Food, Drug, and Cosmetic Act, 21 U.S.C. Sec.
355, to the extent the conduct with respect to the substance is permitted by the exemption;
(D) any substance to the extent not intended for human consumption before an exemption
takes effect with respect to the substance;
(E) any drug intended for lawful use in the diagnosis, cure, mitigation, treatment, or prevention
of disease in humans or other animals, which contains ephedrine, pseudoephedrine,
norpseudoephedrine, or phenylpropanolamine if the drug is lawfully purchased, sold,
transferred, or furnished as an over-the-counter medication without prescription; or
(F) dietary supplements, vitamins, minerals, herbs, or other similar substances including
concentrates or extracts, which are not otherwise regulated by law, which may contain
naturally occurring amounts of chemicals or substances listed in this chapter, or in rules
made in accordance with Title 63G, Chapter 3, Utah Administrative Rulemaking Act.50f716ce90997667(e)
(i) “Controlled substance” means a drug or substance:
(A) included in Schedules I, II, III, IV, or V of Section 58-37-108;
(B) included in Schedules I, II, III, IV, or V of the federal Controlled Substances Act, Title II,
P.L. 91-513;
(C) that is a controlled substance analog; or
(D) listed in Section 58-37-109.
58-37-107 Controlled substances.
Page 10
Utah Code
(1) All substances listed in Section 58-37-108 or 58-37-109 are controlled.
(2) All substances listed in the federal Controlled Substances Act, Title II, P.L. 91-513, are
controlled.
b63b983ce62e2b82(f)
(i) “Controlled substance analog” means:
(A) a substance the chemical structure of which is substantially similar to the chemical
structure of a controlled substance listed in Schedules I and II of Section 58-37-108, a
substance listed in Section 58-37-109, or in Schedules I and II of the federal Controlled
Substances Act, Title II, P.L. 91-513;
(B) a substance that has a stimulant, depressant, or hallucinogenic effect on the central
nervous system substantially similar to the stimulant, depressant, or hallucinogenic
effect on the central nervous system of controlled substances listed in Schedules I and
II of Section 58-37-108, substances listed in Section 58-37-109, or substances listed in
Schedules I and II of the federal Controlled Substances Act, Title II, P.L. 91-513; or
(C) a substance that, with respect to a particular individual, is represented or intended to
have a stimulant, depressant, or hallucinogenic effect on the central nervous system
substantially similar to the stimulant, depressant, or hallucinogenic effect on the central
nervous system of controlled substances listed in Schedules I and II of Section 58-37-108,
substances listed in Section 58-37-109, or substances listed in Schedules I and II of the
federal Controlled Substances Act, Title II, P.L. 91-513.
76-18-207 Unlawfully possessing or using a controlled substance or controlled substance
analog.
(1)
(a) As used in this section:
(i) “Correctional facility” means the same as that term is defined in Section 64-13-1.
(ii) “Good faith” does not include seeking medical assistance under this section during the
course of a law enforcement agency’s execution of a search warrant, execution of an arrest
warrant, or other lawful search.
(b) Terms defined in Sections 58-37-101, 76-1-101.5, 76-18-101, and 76-18-201 apply to this
section.
(2) An actor commits unlawfully possessing or using a controlled substance or a controlled
substance analog if the actor knowingly and intentionally possesses or uses a controlled
substance or a controlled substance analog, unless the controlled substance or controlled
substance analog was obtained:
(a) under a valid prescription or order;
(b) directly from a practitioner while acting in the course of the practitioner’s professional practice;
or
(c) as otherwise authorized by this part or Title 58, Chapter 37, Controlled Substances.
819d91abcb6742f558-37-108 Schedules of controlled substances -- Schedules I through V -- Findings required -- Specific substances included in schedules. (1) There are established five schedules of controlled substances known as Schedules I, II, III, IV, and V, which consist of substances listed in this section. (2) Schedules I, II, III, IV, and V consist of the following drugs or other substances by the official name, common or usual name, chemical name, or brand name designated: (a) Except as provided in Subsection (3), Schedule I: (i) Unless specifically excepted or unless listed in another schedule, any of the following opiates, including their isomers, esters, ethers, salts, and salts of isomers, esters, and ethers, when the existence of the isomers, esters, ethers, and salts is possible within the specific chemical designation: (A) Acetyl-alpha-methylfentanyl (N-[1-(1-methyl-2-phenethyl)-4-piperidinyl]-N- phenylacetamide); (B) Acetyl fentanyl: (N-(1-phenethylpiperidin-4-yl)-N-phenylacetamide); (C) Acetylmethadol; (D) Acryl fentanyl (N-(1-Phenethylpiperidin-4-yl)-N-phenylacrylamide); (E) Allylprodine; (F) Alphacetylmethadol, except levo-alphacetylmethadol also known as levo-alpha- acetylmethadol, levomethadyl acetate, or LAAM; (G) Alphameprodine; (H) Alphamethadol; (I) Alpha-methylfentanyl (N-[1-(alpha-methyl-beta-phenyl)ethyl-4-piperidyl] propionanilide; 1- (1-methyl-2-phenylethyl)-4-(N-propanilido) piperidine); (J) Alpha-methylthiofentanyl (N-[1-methyl-2-(2-thienyl)ethyl-4- piperidinyl]-N- phenylpropanamide); (K) Benzylpiperazine; (L) Benzethidine; (M) Betacetylmethadol; (N) Beta-hydroxyfentanyl (N-[1-(2-hydroxy-2-phenethyl)-4- piperidinyl]-N- phenylpropanamide); (O) Beta-hydroxy-3-methylfentanyl, other name: N-[1-(2-hydroxy-2- phenethyl)-3-methyl-4- piperidinyl]-N-phenylpropanamide; (P) Betameprodine; (Q) Betamethadol; (R) Betaprodine; (S) Butyryl fentanyl (N-(1-(2-phenylethyl)-4-piperidinyl)-N-phenylbutyramide); (T) Clonitazene; (U) Cyclopropyl fentanyl (N-(1-Phenethylpiperidin-4-yl)-N-phenylcyclopropanecarboxamide); (V) Dextromoramide; (W) Diampromide; (X) Diethylthiambutene; (Y) Difenoxin; Page 11 Utah Code (Z) Dimenoxadol; (AA) Dimepheptanol; (BB) Dimethylthiambutene; (CC) Dioxaphetyl butyrate; (DD) Dipipanone; (EE) Ethylmethylthiambutene; (FF) Etizolam (1-Methyl-6-o-chlorophenyl-8-ethyl-4H-s-triazolo[3,4-c]thieno[2,3-e]1,4- diazepine); (GG) Etonitazene; (HH) Etoxeridine; (II) Furanyl fentanyl (N-phenyl-N-[1-(2-phenylethyl)piperidin-4-yl] furan-2-carboxamide); (JJ) Furethidine; (KK) Hydroxypethidine; (LL) Ketobemidone; (MM) Levomoramide; (NN) Levophenacylmorphan; (OO) Methoxyacetyl fentanyl (2-Methoxy-N-(1-phenylethylpiperidinyl-4-yl)-N-acetamide); (PP) Morpheridine; (QQ) MPPP (1-methyl-4-phenyl-4-propionoxypiperidine); (RR) Noracymethadol; (SS) Norlevorphanol; (TT) Normethadone; (UU) Norpipanone; (VV) Para-fluorofentanyl (N-(4-fluorophenyl)-N-[1-(2-phenethyl)-4- piperidinyl] propanamide); (WW) Para-fluoroisobutyryl fentanyl (N-(4-Fluorophenyl)-N-(1-phenethylpiperidin-4- yl)isobutyramide); (XX) PEPAP (1-(-2-phenethyl)-4-phenyl-4-acetoxypiperidine); (YY) Phenadoxone; (ZZ) Phenampromide; (AAA) Phenibut; (BBB) Phenomorphan; (CCC) Phenoperidine; (DDD) Piritramide; (EEE) Proheptazine; (FFF) Properidine; (GGG) Propiram; (HHH) Racemoramide; (III) Tetrahydrofuran fentanyl (N-(1-Phenethylpiperidin-4-yl)-N-phenyltetrahydrofuran-2- carboxamide); (JJJ) Thiofentanyl (N-phenyl-N-[1-(2-thienyl)ethyl-4-piperidinyl]- propanamide; (KKK) Tianeptine; (LLL) Tilidine; (MMM) Trimeperidine; (NNN) 3-methylfentanyl, including the optical and geometric isomers (N-[3-methyl-1-(2- phenylethyl)-4-piperidyl]- N-phenylpropanamide); (OOO) 3-methylthiofentanyl (N-[(3-methyl-1-(2-thienyl)ethyl-4-piperidinyl]-N- phenylpropanamide); Page 12 Utah Code (PPP) 3,4-dichloro-N-[2-(dimethylamino)cyclohexyl]-N-methylbenzamide also known as U-47700; and (QQQ) 4-cyano CUMYL-BUTINACA. (ii) Unless specifically excepted or unless listed in another schedule, any of the following opium derivatives, their salts, isomers, and salts of isomers when the existence of the salts, isomers, and salts of isomers is possible within the specific chemical designation: (A) Acetorphine; (B) Acetyldihydrocodeine; (C) Benzylmorphine; (D) Codeine methylbromide; (E) Codeine-N-Oxide; (F) Cyprenorphine; (G) Desomorphine; (H) Dihydromorphine; (I) Drotebanol; (J) Etorphine (except hydrochloride salt); (K) Heroin; (L) Hydromorphinol; (M) Methyldesorphine; (N) Methylhydromorphine; (O) Morphine methylbromide; (P) Morphine methylsulfonate; (Q) Morphine-N-Oxide; (R) Myrophine; (S) Nicocodeine; (T) Nicomorphine; (U) Normorphine; (V) Pholcodine; and (W) Thebacon. (iii) Unless specifically excepted or unless listed in another schedule, any material, compound, mixture, or preparation that contains any quantity of the following hallucinogenic substances, or that contains any of their salts, isomers, and salts of isomers when the existence of the salts, isomers, and salts of isomers is possible within the specific chemical designation; as used in this Subsection (2)(a)(iii) only, "isomer" includes the optical, position, and geometric isomers: (A) Alpha-ethyltryptamine, some trade or other names: etryptamine; Monase; α-ethyl-1H- indole-3-ethanamine; 3-(2-aminobutyl) indole; α-ET; and AET; (B) 4-bromo-2,5-dimethoxy-amphetamine, some trade or other names: 4-bromo-2,5- dimethoxy-α-methylphenethylamine; 4-bromo-2,5-DMA; (C) 4-bromo-2,5-dimethoxyphenethylamine, some trade or other names: 2-(4-bromo-2,5- dimethoxyphenyl)-1-aminoethane; alpha-desmethyl DOB; 2C-B, Nexus; (D) 2,5-dimethoxyamphetamine, some trade or other names: 2,5-dimethoxy-α- methylphenethylamine; 2,5-DMA; (E) 2,5-dimethoxy-4-ethylamphetamine, some trade or other names: DOET; (F) 4-methoxyamphetamine, some trade or other names: 4-methoxy-α- methylphenethylamine; paramethoxyamphetamine, PMA; Page 13 Utah Code (G) 5-methoxy-3,4-methylenedioxyamphetamine; (H) 4-methyl-2,5-dimethoxy-amphetamine, some trade and other names: 4-methyl-2,5- dimethoxy-α-methylphenethylamine; “DOM”; and “STP”; (I) 3,4-methylenedioxy amphetamine; (J) 3,4-methylenedioxymethamphetamine (MDMA); (K) 3,4-methylenedioxy-N-ethylamphetamine, also known as N-ethyl- alpha- methyl-3,4(methylenedioxy)phenethylamine, N-ethyl MDA, MDE, MDEA; (L) N-hydroxy-3,4-methylenedioxyamphetamine, also known as N-hydroxy-alpha- methyl-3,4(methylenedioxy)phenethylamine, and N-hydroxy MDA; (M) 3,4,5-trimethoxy amphetamine; (N) Bufotenine, some trade and other names: 3-(β-Dimethylaminoethyl)-5-hydroxyindole; 3-(2-dimethylaminoethyl)-5-indolol; N, N-dimethylserotonin; 5-hydroxy-N,N- dimethyltryptamine; mappine; (O) Diethyltryptamine, some trade and other names: N,N-Diethyltryptamine; DET; (P) Dimethyltryptamine, some trade or other names: DMT; (Q) Ibogaine, some trade and other names: 7-Ethyl-6,6β,7,8,9,10,12,13-octahydro-2- methoxy-6,9-methano-5H-pyrido [1', 2':1,2] azepino [5,4-b] indole; Tabernanthe iboga; (R) Lysergic acid diethylamide; (S) Marijuana; (T) Mescaline; (U) Parahexyl, some trade or other names: 3-Hexyl-1-hydroxy-7,8,9,10-tetrahydro-6,6,9- trimethyl-6H-dibenzo[b,d]pyran; Synhexyl; (V) Peyote, meaning all parts of the plant presently classified botanically as Lophophora williamsii Lemaire, whether growing or not, the seeds thereof, any extract from any part of such plant, and every compound, manufacture, salts, derivative, mixture, or preparation of such plant, its seeds or extracts (Interprets 21 USC 812(c), Schedule I(c) (12)); (W) N-ethyl-3-piperidyl benzilate; (X) N-methyl-3-piperidyl benzilate; (Y) Psilocybin; (Z) Psilocyn; (AA) Tetrahydrocannabinols, naturally contained in a plant of the genus Cannabis (cannabis plant), except for marijuana as defined in Subsection 58-37-101(1)(w)(i)(E), as well as synthetic equivalents of the substances contained in the cannabis plant, or in the resinous extractives of Cannabis, sp. and/or synthetic substances, derivatives, and their isomers with similar chemical structure and pharmacological activity to those substances contained in the plant, such as the following: ∆1 cis or trans tetrahydrocannabinol, and their optical isomers ∆6 cis or trans tetrahydrocannabinol, and their optical isomers ∆3,4 cis or trans tetrahydrocannabinol, and its optical isomers, and since nomenclature of these substances is not internationally standardized, compounds of these structures, regardless of numerical designation of atomic positions covered; (BB) Ethylamine analog of phencyclidine, some trade or other names: N- ethyl-1-phenylcyclohexylamine, (1-phenylcyclohexyl)ethylamine, N-(1- phenylcyclohexyl)ethylamine, cyclohexamine, PCE; (CC) Pyrrolidine analog of phencyclidine, some trade or other names: 1-(1-phenylcyclohexyl)- pyrrolidine, PCPy, PHP; Page 14 Utah Code (DD) Thiophene analog of phencyclidine, some trade or other names: 1-[1-(2-thienyl)- cyclohexyl]-piperidine, 2-thienylanalog of phencyclidine, TPCP, TCP; and (EE) 1-[1-(2-thienyl)cyclohexyl]pyrrolidine, some other names: TCPy. (iv) Unless specifically excepted or unless listed in another schedule, any material compound, mixture, or preparation that contains any quantity of the following substances having a depressant effect on the central nervous system, including its salts, isomers, and salts of isomers when the existence of the salts, isomers, and salts of isomers is possible within the specific chemical designation: (A) Mecloqualone; and (B) Methaqualone. (v) Any material, compound, mixture, or preparation containing any quantity of the following substances having a stimulant effect on the central nervous system, including their salts, isomers, and salts of isomers: (A) Aminorex, some other names: aminoxaphen; 2-amino-5-phenyl-2-oxazoline; or 4,5- dihydro-5-phenyl-2-oxazolamine; (B) Cathinone, some trade or other names: 2-amino-1-phenyl-1-propanone, alpha- aminopropiophenone, 2-aminopropiophenone, and norephedrone; (C) Fenethylline; (D) Methcathinone, some other names: 2-(methylamino)-propiophenone; alpha- (methylamino)propiophenone; 2-(methylamino)-1-phenylpropan-1-one; alpha-N- methylaminopropiophenone; monomethylpropion; ephedrone; N-methylcathinone; methylcathinone; AL-464; AL-422; AL-463 and UR1432, its salts, optical isomers, and salts of optical isomers; (E) (±)cis-4-methylaminorex ((±)cis-4,5-dihydro-4-methyl-5-phenyl-2-oxazolamine); (F) N-ethylamphetamine; and (G) N,N-dimethylamphetamine, also known as N,N-alpha-trimethyl-benzeneethanamine; N,N- alpha-trimethylphenethylamine. (vi) Any material, compound, mixture, or preparation that contains any quantity of the following substances, including their optical isomers, salts, and salts of isomers, subject to temporary emergency scheduling: (A) N-[1-benzyl-4-piperidyl]-N-phenylpropanamide (benzylfentanyl); and (B) N-[1- (2-thienyl)methyl-4-piperidyl]-N-phenylpropanamide (thenylfentanyl). (vii) Unless specifically excepted or unless listed in another schedule, any material, compound, mixture, or preparation that contains any quantity of gamma hydroxy butyrate (gamma hydrobutyric acid), including its salts, isomers, and salts of isomers. (viii) Unless specifically excepted or unless listed in another schedule, the following substances commonly found in Mitragyna speciosa, including synthetic versions, isomers, esters, ethers, salts, and salts of isomers, esters, and ethers, when the existence of the isomers, esters, ethers, and salts is possible within the specific chemical designation: (A) 7-hydroxymitragynine (methyl (E)-2[(2S,3S,7aS,12bS)-3-ethyl-7a-hydroxy-8- methoxy-2,3,4,6,7,12b-hexahydro-1H-indolo[2,3-a]quinolizin-2-yl]-3-methoxyprop-2- enoate); and (B) Mitragynine pseudoindoxyl (methyl (E)-2-[(2S,6'S,7'S,8'aS)-6'-ethyl-4-methoxy-3- oxospiro[1H-indole-2,1'-3,5,6,7,8,8a-hexahydro-2H-indolizine]-7'-yl]-3-methoxyprop-2- enoate). (b) Schedule II: (i) Unless specifically excepted or unless listed in another schedule, any of the following substances whether produced directly or indirectly by extraction from substances of Page 15 Utah Code vegetable origin, or independently by means of chemical synthesis, or by a combination of extraction and chemical synthesis: (A) Opium and opiate, and any salt, compound, derivative, or preparation of opium or opiate, excluding apomorphine, dextrorphan, nalbuphine, nalmefene, naloxone, and naltrexone, and their respective salts, but including: (I) Raw opium; (II) Opium extracts; (III) Opium fluid; (IV) Powdered opium; (V) Granulated opium; (VI) Tincture of opium; (VII) Codeine; (VIII) Ethylmorphine; (IX) Etorphine hydrochloride; (X) Hydrocodone; (XI) Hydromorphone; (XII) Metopon; (XIII) Morphine; (XIV) Oxycodone; (XV) Oxymorphone; and (XVI) Thebaine; (B) Any salt, compound, derivative, or preparation that is chemically equivalent or identical with any of the substances referred to in Subsection (2)(b)(i)(A), except that these substances may not include the isoquinoline alkaloids of opium; (C) Opium poppy and poppy straw; (D) Coca leaves and any salt, compound, derivative, or preparation of coca leaves, and any salt, compound, derivative, or preparation that is chemically equivalent or identical with any of these substances, and includes cocaine and ecgonine, their salts, isomers, derivatives, and salts of isomers and derivatives, whether derived from the coca plant or synthetically produced, except the substances may not include decocainized coca leaves or extraction of coca leaves, which extractions do not contain cocaine or ecgonine; and (E) Concentrate of poppy straw, which means the crude extract of poppy straw in either liquid, solid, or powder form that contains the phenanthrene alkaloids of the opium poppy. (ii) Unless specifically excepted or unless listed in another schedule, any of the following opiates, including their isomers, esters, ethers, salts, and salts of isomers, esters, and ethers, when the existence of the isomers, esters, ethers, and salts is possible within the specific chemical designation, except dextrorphan and levopropoxyphene: (A) Alfentanil; (B) Alphaprodine; (C) Anileridine; (D) Bezitramide; (E) Bulk dextropropoxyphene (nondosage forms); (F) Carfentanil; (G) Dihydrocodeine; (H) Diphenoxylate; (I) Fentanyl; (J) Isomethadone; Page 16 Utah Code (K) Levo-alphacetylmethadol, some other names: levo-alpha-acetylmethadol, levomethadyl acetate, or LAAM; (L) Levomethorphan; (M) Levorphanol; (N) Metazocine; (O) Methadone; (P) Methadone-Intermediate, 4-cyano-2-dimethylamino-4, 4-diphenyl butane; (Q) Moramide-Intermediate, 2-methyl-3-morpholino-1, 1-diphenylpropane-carboxylic acid; (R) Pethidine (meperidine); (S) Pethidine-Intermediate-A, 4-cyano-1-methyl-4-phenylpiperidine; (T) Pethidine-Intermediate-B, ethyl-4-phenylpiperidine-4-carboxylate; (U) Pethidine-Intermediate-C, 1-methyl-4-phenylpiperidine-4-carboxylic acid; (V) Phenazocine; (W) Piminodine; (X) Racemethorphan; (Y) Racemorphan; (Z) Remifentanil; and (AA) Sufentanil. (iii) Unless specifically excepted or unless listed in another schedule, any material, compound, mixture, or preparation that contains any quantity of the following substances having a stimulant effect on the central nervous system: (A) Amphetamine, its salts, optical isomers, and salts of its optical isomers; (B) Methamphetamine, its salts, isomers, and salts of its isomers; (C) Phenmetrazine and its salts; and (D) Methylphenidate. (iv) Unless specifically excepted or unless listed in another schedule, any material, compound, mixture, or preparation that contains any quantity of the following substances having a depressant effect on the central nervous system, including its salts, isomers, and salts of isomers when the existence of the salts, isomers, and salts of isomers is possible within the specific chemical designation: (A) Amobarbital; (B) Glutethimide; (C) Pentobarbital; (D) Phencyclidine; (E) Phencyclidine immediate precursors: 1-phenylcyclohexylamine and 1- piperidinocyclohexanecarbonitrile (PCC); and (F) Secobarbital. (v) (A) Unless specifically excepted or unless listed in another schedule, any material, compound, mixture, or preparation that contains any quantity of Phenylacetone. (B) Some of these substances may be known by trade or other names: phenyl-2-propanone; P2P; benzyl methyl ketone; and methyl benzyl ketone. (vi) Nabilone, another name for nabilone: (±)-trans-3-(1,1-dimethylheptyl)-6,6a,7,8,10,10a- hexahydro-1-hydroxy-6, 6-dimethyl-9H-dibenzo[b,d]pyran-9-one. (vii) A drug product or preparation that contains any component of marijuana, including tetrahydrocannabinol, and is approved by the United States Food and Drug Administration and scheduled by the Drug Enforcement Administration in Schedule II of the federal Controlled Substances Act, Title II, P.L. 91-513. Page 17 Utah Code (c) Schedule III: (i) Unless specifically excepted or unless listed in another schedule, any material, compound, mixture, or preparation that contains any quantity of the following substances having a stimulant effect on the central nervous system, including its salts, isomers whether optical, position, or geometric, and salts of the isomers when the existence of the salts, isomers, and salts of isomers is possible within the specific chemical designation: (A) those compounds, mixtures, or preparations in dosage unit form containing any stimulant substances listed in Schedule II, which compounds, mixtures, or preparations were listed on August 25, 1971, as excepted compounds under Section 1308.32 of Title 21 of the Code of Federal Regulations, and any other drug of the quantitive composition shown in that list for those drugs or that is the same except that it contains a lesser quantity of controlled substances; (B) Benzphetamine; (C) Chlorphentermine; (D) Clortermine; and (E) Phendimetrazine. (ii) Unless specifically excepted or unless listed in another schedule, any material, compound, mixture, or preparation that contains any quantity of the following substances having a depressant effect on the central nervous system: (A) any compound, mixture, or preparation containing amobarbital, secobarbital, pentobarbital, or any salt of any of them, and one or more other active medicinal ingredients that are not listed in any schedule; (B) any suppository dosage form containing amobarbital, secobarbital, or pentobarbital, or any salt of any of these drugs that is approved by the United States Food and Drug Administration for marketing only as a suppository; (C) any substance that contains any quantity of a derivative of barbituric acid or any salt of any of them; (D) Chlorhexadol; (E) Buprenorphine; (F) any drug product containing gamma hydroxybutyric acid, including its salts, isomers, and salts of isomers, for which an application is approved under the federal Food, Drug, and Cosmetic Act, Section 505; (G) Ketamine, its salts, isomers, and salts of isomers, some other names for ketamine: ± -2- (2-chlorophenyl)-2-(methylamino)-cyclohexanone; (H) Lysergic acid; (I) Lysergic acid amide; (J) Methyprylon; (K) Sulfondiethylmethane; (L) Sulfonethylmethane; (M) Sulfonmethane; and (N) Tiletamine and zolazepam or any of their salts, some trade or other names for a tiletamine-zolazepam combination product: Telazol, some trade or other names for tiletamine: 2-(ethylamino)-2-(2-thienyl)-cyclohexanone, some trade or other names for zolazepam: 4-(2-fluorophenyl)-6,8-dihydro-1,3,8-trimethylpyrazolo-[3,4-e] [1,4]- diazepin-7(1H)-one, flupyrazapon. (iii) Dronabinol (synthetic) in sesame oil and encapsulated in a soft gelatin capsule in a U.S. Food and Drug Administration approved drug product, some other names for dronabinol: Page 18 Utah Code (6aR-trans)-6a,7,8,10a-tetrahydro-6,6,9-trimethyl-3-pentyl-6H-dibenzo[b,d]pyran-1-ol, or (-)- delta-9-(trans)-tetrahydrocannabinol. (iv) Nalorphine. (v) Unless specifically excepted or unless listed in another schedule, any material, compound, mixture, or preparation containing limited quantities of any of the following narcotic drugs, or their salts calculated as the free anhydrous base or alkaloid: (A) Not more than 1.8 grams of codeine per 100 milliliters or not more than 90 milligrams per dosage unit, with an equal or greater quantity of an isoquinoline alkaloid of opium; (B) Not more than 1.8 grams of codeine per 100 milliliters or not more than 90 milligrams per dosage unit, with one or more active non-narcotic ingredients in recognized therapeutic amounts; (C) Not more than 300 milligrams of dihydrocodeinone per 100 milliliters or not more than 15 milligrams per dosage unit, with a fourfold or greater quantity of an isoquinoline alkaloid of opium; (D) Not more than 300 milligrams of dihydrocodeinone per 100 milliliters or not more than 15 milligrams per dosage unit, with one or more active, non-narcotic ingredients in recognized therapeutic amounts; (E) Not more than 1.8 grams of dihydrocodeine per 100 milliliters or not more than 90 milligrams per dosage unit, with one or more active non-narcotic ingredients in recognized therapeutic amounts; (F) Not more than 300 milligrams of ethylmorphine per 100 milliliters or not more than 15 milligrams per dosage unit, with one or more active, non-narcotic ingredients in recognized therapeutic amounts; (G) Not more than 500 milligrams of opium per 100 milliliters or per 100 grams, or not more than 25 milligrams per dosage unit, with one or more active, non-narcotic ingredients in recognized therapeutic amounts; and (H) Not more than 50 milligrams of morphine per 100 milliliters or per 100 grams with one or more active, non-narcotic ingredients in recognized therapeutic amounts. (vi) Unless specifically excepted or unless listed in another schedule, anabolic steroids including any of the following or any isomer, ester, salt, or derivative of the following that promotes muscle growth: (A) Boldenone; (B) Chlorotestosterone (4-chlortestosterone); (C) Clostebol; (D) Dehydrochlormethyltestosterone; (E) Dihydrotestosterone (4-dihydrotestosterone); (F) Drostanolone; (G) Ethylestrenol; (H) Fluoxymesterone; (I) Formebulone (formebolone); (J) Mesterolone; (K) Methandienone; (L) Methandranone; (M) Methandriol; (N) Methandrostenolone; (O) Methenolone; (P) Methyltestosterone; (Q) Mibolerone; Page 19 Utah Code (R) Nandrolone; (S) Norethandrolone; (T) Oxandrolone; (U) Oxymesterone; (V) Oxymetholone; (W) Stanolone; (X) Stanozolol; (Y) Testolactone; (Z) Testosterone; and (AA) Trenbolone. (vii) Anabolic steroids expressly intended for administration through implants to cattle or other nonhuman species, and approved by the Secretary of Health and Human Services for use, may not be classified as a controlled substance. (viii) A drug product or preparation that contains any component of marijuana, including tetrahydrocannabinol, and is approved by the United States Food and Drug Administration and scheduled by the Drug Enforcement Administration in Schedule III of the federal Controlled Substances Act, Title II, P.L. 91-513. (ix) Nabiximols. (d) Schedule IV: (i) Unless specifically excepted or unless listed in another schedule, any material, compound, mixture, or preparation containing not more than 1 milligram of difenoxin and not less than 25 micrograms of atropine sulfate per dosage unit, or any salts of any of them. (ii) Unless specifically excepted or unless listed in another schedule, any material, compound, mixture, or preparation that contains any quantity of the following substances, including its salts, isomers, and salts of isomers when the existence of the salts, isomers, and salts of isomers is possible within the specific chemical designation: (A) Alprazolam; (B) Barbital; (C) Bromazepam; (D) Butorphanol; (E) Camazepam; (F) Carisoprodol; (G) Chloral betaine; (H) Chloral hydrate; (I) Chlordiazepoxide; (J) Clobazam; (K) Clonazepam; (L) Clorazepate; (M) Clotiazepam; (N) Cloxazolam; (O) Delorazepam; (P) Diazepam; (Q) Dichloralphenazone; (R) Estazolam; (S) Ethchlorvynol; (T) Ethinamate; (U) Ethyl loflazepate; (V) Fludiazepam; Page 20 Utah Code (W) Flunitrazepam; (X) Flurazepam; (Y) Halazepam; (Z) Haloxazolam; (AA) Ketazolam; (BB) Loprazolam; (CC) Lorazepam; (DD) Lormetazepam; (EE) Mebutamate; (FF) Medazepam; (GG) Meprobamate; (HH) Methohexital; (II) Methylphenobarbital (mephobarbital); (JJ) Midazolam; (KK) Nimetazepam; (LL) Nitrazepam; (MM) Nordiazepam; (NN) Oxazepam; (OO) Oxazolam; (PP) Paraldehyde; (QQ) Pentazocine; (RR) Petrichloral; (SS) Phenobarbital; (TT) Pinazepam; (UU) Prazepam; (VV) Quazepam; (WW) Temazepam; (XX) Tetrazepam; (YY) Tramadol; (ZZ) Triazolam; (AAA) Zaleplon; and (BBB) Zolpidem. (iii) Any material, compound, mixture, or preparation of fenfluramine that contains any quantity of the following substances, including its salts, isomers whether optical, position, or geometric, and salts of the isomers when the existence of the salts, isomers, and salts of isomers is possible. (iv) Unless specifically excepted or unless listed in another schedule, any material, compound, mixture, or preparation that contains any quantity of the following substances having a stimulant effect on the central nervous system, including its salts, isomers whether optical, position, or geometric isomers, and salts of the isomers when the existence of the salts, isomers, and salts of isomers is possible within the specific chemical designation: (A) Cathine ((+)-norpseudoephedrine); (B) Diethylpropion; (C) Fencamfamine; (D) Fenproprex; (E) Mazindol; (F) Mefenorex; (G) Modafinil; Page 21 Utah Code (H) Pemoline, including organometallic complexes and chelates thereof; (I) Phentermine; (J) Pipradrol; (K) Sibutramine; and (L) SPA ((-)-1-dimethylamino-1,2-diphenylethane). (v) Unless specifically excepted or unless listed in another schedule, any material, compound, mixture, or preparation that contains any quantity of dextropropoxyphene (alpha-(+)-4- dimethylamino-1, 2-diphenyl-3-methyl-2-propionoxybutane), including its salts. (vi) A drug product or preparation that contains any component of marijuana and is approved by the United States Food and Drug Administration and scheduled by the Drug Enforcement Administration in Schedule IV of the federal Controlled Substances Act, Title II, P.L. 91-513. (e) Schedule V: (i) Any compound, mixture, or preparation containing any of the following limited quantities of narcotic drugs, or their salts calculated as the free anhydrous base or alkaloid, which includes one or more non-narcotic active medicinal ingredients in sufficient proportion to confer upon the compound, mixture, or preparation valuable medicinal qualities other than those possessed by the narcotic drug alone: (A) not more than 200 milligrams of codeine per 100 milliliters or per 100 grams; (B) not more than 100 milligrams of dihydrocodeine per 100 milliliters or per 100 grams; (C) not more than 100 milligrams of ethylmorphine per 100 milliliters or per 100 grams; (D) not more than 2.5 milligrams of diphenoxylate and not less than 25 micrograms of atropine sulfate per dosage unit; (E) not more than 100 milligrams of opium per 100 milliliters or per 100 grams; (F) not more than 0.5 milligram of difenoxin and not less than 25 micrograms of atropine sulfate per dosage unit; and (G) unless specifically exempted or excluded or unless listed in another schedule, any material, compound, mixture, or preparation that contains Pyrovalerone having a stimulant effect on the central nervous system, including its salts, isomers, and salts of isomers. (ii) A drug product or preparation that contains any component of marijuana, including cannabidiol, and is approved by the United States Food and Drug Administration and scheduled by the Drug Enforcement Administration in Schedule V of the federal Controlled Substances Act, Title II, P.L. 91-513. (iii) Gabapentin. (3) (a) As used in this subsection, "pharmaceutical composition" means a drug that has United States Food and Drug Administration approval under 21 U.S.C. Sec. 355 following clinical trials. (b) If the federal government schedules a pharmaceutical composition of a Schedule I controlled substance or a pharmaceutical composition of any form of a Schedule I controlled substance in a schedule that is not Schedule I, that pharmaceutical composition is deemed scheduled under this section in the same schedule that the pharmaceutical composition is scheduled under 21 U.S.C. Sec. 812 and 21 C.F.R. Part 1308. Renumbered and Amended by Chapter 362, 2026 General Session
46a31071bfabc52a(2) Schedules I, II, III, IV, and V consist of the following drugs or other substances by the official name, common or usual name, chemical name, or brand name designated: (a) Except as provided in Subsection (3), Schedule I: (i) Unless specifically excepted or unless listed in another schedule, any of the following opiates, including their isomers, esters, ethers, salts, and salts of isomers, esters, and ethers, when the existence of the isomers, esters, ethers, and salts is possible within the specific chemical designation: (A) Acetyl-alpha-methylfentanyl (N-[1-(1-methyl-2-phenethyl)-4-piperidinyl]-N- phenylacetamide); (B) Acetyl fentanyl: (N-(1-phenethylpiperidin-4-yl)-N-phenylacetamide); (C) Acetylmethadol; (D) Acryl fentanyl (N-(1-Phenethylpiperidin-4-yl)-N-phenylacrylamide); (E) Allylprodine; (F) Alphacetylmethadol, except levo-alphacetylmethadol also known as levo-alpha- acetylmethadol, levomethadyl acetate, or LAAM; (G) Alphameprodine; (H) Alphamethadol; (I) Alpha-methylfentanyl (N-[1-(alpha-methyl-beta-phenyl)ethyl-4-piperidyl] propionanilide; 1- (1-methyl-2-phenylethyl)-4-(N-propanilido) piperidine); (J) Alpha-methylthiofentanyl (N-[1-methyl-2-(2-thienyl)ethyl-4- piperidinyl]-N- phenylpropanamide); (K) Benzylpiperazine; (L) Benzethidine; (M) Betacetylmethadol; (N) Beta-hydroxyfentanyl (N-[1-(2-hydroxy-2-phenethyl)-4- piperidinyl]-N- phenylpropanamide); (O) Beta-hydroxy-3-methylfentanyl, other name: N-[1-(2-hydroxy-2- phenethyl)-3-methyl-4- piperidinyl]-N-phenylpropanamide; (P) Betameprodine; (Q) Betamethadol; (R) Betaprodine; (S) Butyryl fentanyl (N-(1-(2-phenylethyl)-4-piperidinyl)-N-phenylbutyramide); (T) Clonitazene; (U) Cyclopropyl fentanyl (N-(1-Phenethylpiperidin-4-yl)-N-phenylcyclopropanecarboxamide); (V) Dextromoramide; (W) Diampromide; (X) Diethylthiambutene; (Y) Difenoxin; (Z) Dimenoxadol; (AA) Dimepheptanol; (BB) Dimethylthiambutene; (CC) Dioxaphetyl butyrate; (DD) Dipipanone; (EE) Ethylmethylthiambutene; (FF) Etizolam (1-Methyl-6-o-chlorophenyl-8-ethyl-4H-s-triazolo[3,4-c]thieno[2,3-e]1,4- diazepine); (GG) Etonitazene; (HH) Etoxeridine; (II) Furanyl fentanyl (N-phenyl-N-[1-(2-phenylethyl)piperidin-4-yl] furan-2-carboxamide); (JJ) Furethidine; (KK) Hydroxypethidine; (LL) Ketobemidone; (MM) Levomoramide; (NN) Levophenacylmorphan; (OO) Methoxyacetyl fentanyl (2-Methoxy-N-(1-phenylethylpiperidinyl-4-yl)-N-acetamide); (PP) Morpheridine; (QQ) MPPP (1-methyl-4-phenyl-4-propionoxypiperidine); (RR) Noracymethadol; (SS) Norlevorphanol; (TT) Normethadone; (UU) Norpipanone; (VV) Para-fluorofentanyl (N-(4-fluorophenyl)-N-[1-(2-phenethyl)-4- piperidinyl] propanamide); (WW) Para-fluoroisobutyryl fentanyl (N-(4-Fluorophenyl)-N-(1-phenethylpiperidin-4- yl)isobutyramide); (XX) PEPAP (1-(-2-phenethyl)-4-phenyl-4-acetoxypiperidine); (YY) Phenadoxone; (ZZ) Phenampromide; (AAA) Phenibut; (BBB) Phenomorphan; (CCC) Phenoperidine; (DDD) Piritramide; (EEE) Proheptazine; (FFF) Properidine; (GGG) Propiram; (HHH) Racemoramide; (III) Tetrahydrofuran fentanyl (N-(1-Phenethylpiperidin-4-yl)-N-phenyltetrahydrofuran-2- carboxamide); (JJJ) Thiofentanyl (N-phenyl-N-[1-(2-thienyl)ethyl-4-piperidinyl]- propanamide; (KKK) Tianeptine; (LLL) Tilidine; (MMM) Trimeperidine; (NNN) 3-methylfentanyl, including the optical and geometric isomers (N-[3-methyl-1-(2- phenylethyl)-4-piperidyl]- N-phenylpropanamide); (OOO) 3-methylthiofentanyl (N-[(3-methyl-1-(2-thienyl)ethyl-4-piperidinyl]-N- phenylpropanamide); (PPP) 3,4-dichloro-N-[2-(dimethylamino)cyclohexyl]-N-methylbenzamide also known as U-47700; and (QQQ) 4-cyano CUMYL-BUTINACA.
9e125ec4f481cc7158-37-108 Schedules of controlled substances -- Schedules I through V -- Findings required
-- Specific substances included in schedules.
(1) There are established five schedules of controlled substances known as Schedules I, II, III, IV,
and V, which consist of substances listed in this section.
(2) Schedules I, II, III, IV, and V consist of the following drugs or other substances by the official
name, common or usual name, chemical name, or brand name designated:
(a) Except as provided in Subsection (3), Schedule I:
(iii) Unless specifically excepted or unless listed in another schedule, any material, compound,
mixture, or preparation that contains any quantity of the following hallucinogenic
substances, or that contains any of their salts, isomers, and salts of isomers when the
existence of the salts, isomers, and salts of isomers is possible within the specific chemical
designation; as used in this Subsection (2)(a)(iii) only, "isomer" includes the optical, position,
and geometric isomers:
(A) Alpha-ethyltryptamine, some trade or other names: etryptamine; Monase; α-ethyl-1H-
indole-3-ethanamine; 3-(2-aminobutyl) indole; α-ET; and AET;
(B) 4-bromo-2,5-dimethoxy-amphetamine, some trade or other names: 4-bromo-2,5-
dimethoxy-α-methylphenethylamine; 4-bromo-2,5-DMA;
(C) 4-bromo-2,5-dimethoxyphenethylamine, some trade or other names: 2-(4-bromo-2,5-
dimethoxyphenyl)-1-aminoethane; alpha-desmethyl DOB; 2C-B, Nexus;
(D) 2,5-dimethoxyamphetamine, some trade or other names: 2,5-dimethoxy-α-
methylphenethylamine; 2,5-DMA;
(E) 2,5-dimethoxy-4-ethylamphetamine, some trade or other names: DOET;
(F) 4-methoxyamphetamine, some trade or other names: 4-methoxy-α-
methylphenethylamine; paramethoxyamphetamine, PMA;
(G) 5-methoxy-3,4-methylenedioxyamphetamine;
(H) 4-methyl-2,5-dimethoxy-amphetamine, some trade and other names: 4-methyl-2,5-
dimethoxy-α-methylphenethylamine; “DOM”; and “STP”;
(I) 3,4-methylenedioxy amphetamine;
(J) 3,4-methylenedioxymethamphetamine (MDMA);
(K) 3,4-methylenedioxy-N-ethylamphetamine, also known as N-ethyl- alpha-
methyl-3,4(methylenedioxy)phenethylamine, N-ethyl MDA, MDE, MDEA;
(L) N-hydroxy-3,4-methylenedioxyamphetamine, also known as N-hydroxy-alpha-
methyl-3,4(methylenedioxy)phenethylamine, and N-hydroxy MDA;
(M) 3,4,5-trimethoxy amphetamine;
(N) Bufotenine, some trade and other names: 3-(β-Dimethylaminoethyl)-5-hydroxyindole;
3-(2-dimethylaminoethyl)-5-indolol; N, N-dimethylserotonin; 5-hydroxy-N,N-
dimethyltryptamine; mappine;
(O) Diethyltryptamine, some trade and other names: N,N-Diethyltryptamine; DET;
(P) Dimethyltryptamine, some trade or other names: DMT;
(Q) Ibogaine, some trade and other names: 7-Ethyl-6,6β,7,8,9,10,12,13-octahydro-2-
methoxy-6,9-methano-5H-pyrido [1', 2':1,2] azepino [5,4-b] indole; Tabernanthe iboga;
(R) Lysergic acid diethylamide;
(S) Marijuana;
(T) Mescaline;
(U) Parahexyl, some trade or other names: 3-Hexyl-1-hydroxy-7,8,9,10-tetrahydro-6,6,9-
trimethyl-6H-dibenzo[b,d]pyran; Synhexyl;
(V) Peyote, meaning all parts of the plant presently classified botanically as Lophophora
williamsii Lemaire, whether growing or not, the seeds thereof, any extract from any part of
such plant, and every compound, manufacture, salts, derivative, mixture, or preparation of
such plant, its seeds or extracts (Interprets 21 USC 812(c), Schedule I(c) (12));
(W) N-ethyl-3-piperidyl benzilate;
(X) N-methyl-3-piperidyl benzilate;
(Y) Psilocybin;
(Z) Psilocyn;
(AA) Tetrahydrocannabinols, naturally contained in a plant of the genus Cannabis (cannabis
plant), except for marijuana as defined in Subsection 58-37-101(1)(w)(i)(E), as well
as synthetic equivalents of the substances contained in the cannabis plant, or in the
resinous extractives of Cannabis, sp. and/or synthetic substances, derivatives, and their
isomers with similar chemical structure and pharmacological activity to those substances
contained in the plant, such as the following: ∆1 cis or trans tetrahydrocannabinol, and
their optical isomers ∆6 cis or trans tetrahydrocannabinol, and their optical isomers ∆3,4
cis or trans tetrahydrocannabinol, and its optical isomers, and since nomenclature of these
substances is not internationally standardized, compounds of these structures, regardless
of numerical designation of atomic positions covered;
(BB) Ethylamine analog of phencyclidine, some trade or other names: N-
ethyl-1-phenylcyclohexylamine, (1-phenylcyclohexyl)ethylamine, N-(1-
phenylcyclohexyl)ethylamine, cyclohexamine, PCE;
(CC) Pyrrolidine analog of phencyclidine, some trade or other names: 1-(1-phenylcyclohexyl)-
pyrrolidine, PCPy, PHP;
(DD) Thiophene analog of phencyclidine, some trade or other names: 1-[1-(2-thienyl)-
cyclohexyl]-piperidine, 2-thienylanalog of phencyclidine, TPCP, TCP; and
(EE) 1-[1-(2-thienyl)cyclohexyl]pyrrolidine, some other names: TCPy.fda440c49eb37c1d(c) Schedule III:
(ii) Unless specifically excepted or unless listed in another schedule, any material, compound,
mixture, or preparation that contains any quantity of the following substances having a
depressant effect on the central nervous system:
(A) any compound, mixture, or preparation containing amobarbital, secobarbital,
pentobarbital, or any salt of any of them, and one or more other active medicinal
ingredients that are not listed in any schedule;
(B) any suppository dosage form containing amobarbital, secobarbital, or pentobarbital,
or any salt of any of these drugs that is approved by the United States Food and Drug
Administration for marketing only as a suppository;
(C) any substance that contains any quantity of a derivative of barbituric acid or any salt of
any of them;
(D) Chlorhexadol;
(E) Buprenorphine;
(F) any drug product containing gamma hydroxybutyric acid, including its salts, isomers, and
salts of isomers, for which an application is approved under the federal Food, Drug, and
Cosmetic Act, Section 505;
(G) Ketamine, its salts, isomers, and salts of isomers, some other names for ketamine: ± -2-
(2-chlorophenyl)-2-(methylamino)-cyclohexanone;7c89669c0128a9b376-9-1110. Abuse of psychotoxic chemical solvent. (1) (a) As used in this section, "psychotoxic chemical solvent" includes any glue, cement, or other substance containing one or more of the following chemical compounds: (i) acetone and acetate; (ii) amyl nitrite or amyl nitrate or their isomers; (iii) benzene, butyl alcohol, butyl nitrite, butyl nitrate, or their isomers; (iv) ethyl alcohol, ethyl nitrite, or ethyl nitrate; (v) ethylene dichloride; (vi) isobutyl alcohol; (vii) methyl alcohol; (viii) methyl ethyl ketone; (ix) n-propyl alcohol; (x) pentachlorophenol; (xi) petroleum ether; (xii) propyl nitrite or propyl nitrate or their isomers; (xiii) toluene; (xiv) xylene; or (xv) another chemical substance capable of causing a condition of intoxication, inebriation, excitement, stupefaction, or the dulling of the brain or nervous system as a result of the inhalation of the fumes or vapors of such chemical substance. (b) Terms defined in Sections 76-1-101.5 and 76-9-1101 apply to this section. (2) Except as provided in Subsection (4) , an actor commits abuse of psychotoxic chemical solvent if: (a) for the purpose of causing a condition of intoxication, inebriation, excitement, stupefaction, or the dulling of the actor’s brain or nervous system, the actor intentionally: (i) smells or inhales the fumes of a psychotoxic chemical solvent; or (ii) possesses, purchases, or attempts to possess or purchase a psychotoxic chemical solvent; or (b) the actor offers, sells, or provides a psychotoxic chemical solvent to another person, knowing that other person or a third party intends to possess or use that psychotoxic chemical solvent in violation of Subsection (2)(a) . (3) A violation of Subsection (2) is a class B misdemeanor. (4) This section does not apply to: (a) the prescribed use, distribution, or sale of a psychotoxic chemical solvent for a medical or dental purpose; or (b) a controlled substance regulated by the provisions of Chapter 18, Part 2, Offenses Concerning Controlled Substances, or Title 58, Chapter 37, Controlled Substances.
9d5a632f71fe8bb876-9-1111. Abuse of nitrous oxide. (1) (a) As used in this section, "nitrous oxide" means: (i) N2O, a colorless gas or liquid that is also referred to as dinitrogen monoxide, nitrogen oxide, or laughing gas; or (ii) any substance containing nitrous oxide. (b) Terms defined in Sections 76-1-101.5 and 76-9-1101 apply to this section. (2) Except as provided in Subsection (4), an actor commits abuse of nitrous oxide if the actor: (a) possesses nitrous oxide with the intent to breathe, inhale, or ingest the nitrous oxide for the purpose of: (i) causing a condition of intoxication, elation, euphoria, dizziness, stupefaction, or dulling of the senses; or (ii) in any manner changing, distorting, or disturbing the audio, visual, or mental processes; (b) knowingly or intentionally is under the influence of nitrous oxide; or (c) offers, sells, or provides nitrous oxide to another person, knowing that other person or a third party intends to possess or use the nitrous oxide in violation of Subsection (2)(a) or (b) . (3) A violation of Subsection (2) is a class A misdemeanor. (4) (a) Subsection (2)(b) does not apply to any person who is under the influence of nitrous oxide pursuant to an administration for the purpose of medical, surgical, or dental care by a person holding a license under state law that authorizes the administration of nitrous oxide. (b) Subsection (2)(c) does not apply to any person who: (i) administers nitrous oxide for the purpose of medical, surgical, or dental care; and (ii) holds a license under state law that authorizes the administration of nitrous oxide.
4e0392801725d222(i) “Controlled substance analog” means: (A) a substance the chemical structure of which is substantially similar to the chemical structure of a controlled substance listed in Schedules I and II of Section 58-37-4, a substance listed in Section 58-37-4.2, or in Schedules I and II of the federal Controlled Substances Act, Title II, P.L. 91-513; (B) a substance that has a stimulant, depressant, or hallucinogenic effect on the central nervous system substantially similar to the stimulant, depressant, or hallucinogenic effect on the central nervous system of controlled substances listed in Schedules I and II of Section 58-37-4, substances listed in Section 58-37-4.2, or substances listed in Schedules I and II of the federal Controlled Substances Act, Title II, P.L. 91-513; or (C) A substance that, with respect to a particular individual, is represented or intended to have a stimulant, depressant, or hallucinogenic effect on the central nervous system substantially similar to the stimulant, depressant, or hallucinogenic effect on the central nervous system of controlled substances listed in Schedules I and II of Section 58-37-4, substances listed in Section 58-37-4.2, or substances listed in Schedules I and II of the federal Controlled Substances Act, Title II, P.L. 91-513. (ii) “Controlled substance analog” does not include: (A) a controlled substance currently scheduled in Schedules I through V of Section 58-37-4; (B) a substance for which there is an approved new drug application; (C) a substance with respect to which an exemption is in effect for investigational use by a particular person under Section 505 of the Food, Drug, and Cosmetic Act, 21 U.S.C. 355, to the extent the conduct with respect to the substance is permitted by the exemption; (D) any substance to the extent not intended for human consumption before an exemption takes effect with respect to the substance; (E) any drug intended for lawful use in the diagnosis, cure, mitigation, treatment, or prevention of disease in man or other animals, which contains ephedrine, pseudoephedrine, norpseudoephedrine, or phenylpropanolamine if the drug is lawfully purchased, sold, transferred, or furnished as an over-the-counter medication without prescription; or (F) dietary supplements, vitamins, minerals, herbs, or other similar substances including concentrates or extracts, which are not otherwise regulated by law, which may contain naturally occurring amounts of chemical or substances listed in this chapter, or in rules adopted pursuant to Title 63G, Chapter 3, Utah Administrative Rulemaking Act.
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