As of November 12, 2026, Kava (Piper methysticum) is legal to sell at retail in Maryland. Not scheduled or named in Maryland law; no kava-specific statute or rule. Controlling source: Md. Code, Crim. Law Sec. 5-402 (Schedule I (controlled dangerous substances)).
Verified November 12, 2026 (hash check) · confidence: confirmedIs Kava Legal? Every state and federal law
Maryland has no free-standing Schedule I list in statute. Crim. Law Sec. 5-402(a) defines Schedule I as controlled dangerous substance analogues, substances the Maryland Department of Health adds under Sec. 5-202(b), and substances designated Schedule I by the federal government unless the Department objects. The Department's rule list (COMAR 10.19.03.20) adds only 4-methoxymethcathinone to Schedule I, and COMAR 10.19.03.02 incorporates 21 CFR 1300–1317, so the operative Schedule I content tracks the federal list, which does not include kava (Piper methysticum). The analogue clause in Sec. 5-402(b) reaches only substances structurally substantially similar to a Schedule I or II substance; no official source applies it to kavalactones. No Maryland statute, rule, prohibited-plant list, kratom act, hemp act or novel-substance law names kava (Piper methysticum). Status: legal, unscheduled; general food and supplement law applies as for any botanical. Not federally controlled (kava is not in 21 CFR 1308.11); FDA dietary supplement and food law apply. See the federal page.
Schedule I consists of each: (1) subsection (b) of this section; controlled dangerous substance analogue, as defined in (2) controlled dangerous substance added to Schedule I by the Department under § 5–202(b) of this title; and (3) controlled dangerous substance designated as a Schedule I controlled dangerous substance by the federal government unless the Department objects under § 5–202(f) of this title.
Among Maryland's 5 neighbors, District of Columbia is restricted; Delaware, Pennsylvania, Virginia and West Virginia are legal.
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Not federally scheduled. Not federally controlled; sold under FDA dietary supplement and food law Federal detail
9 instruments on file for this compound’s framework in Maryland; 4 of 4 citations above are official sources. Each text carries its source and a fingerprint that changes when the law does.
9b6fff1ae0ff7e2b(C) A RETAILER MAY NOT DISTRIBUTE, SELL, OR EXPOSE FOR SALE A PHENIBUT PRODUCT TO AN INDIVIDUAL UNDER THE AGE OF 21 YEARS.
7babe04cfbbd65f0§5–402. (a) Schedule I consists of each: (1) subsection (b) of this section; controlled dangerous substance analogue, as defined in (2) controlled dangerous substance added to Schedule I by the Department under § 5–202(b) of this title; and (3) controlled dangerous substance designated as a Schedule I controlled dangerous substance by the federal government unless the Department objects under § 5–202(f) of this title. (b) (1) In this subsection: substance: (i) “controlled dangerous substance analogue” means a that has a chemical structure substantially similar to the chemical structure of a controlled dangerous substance described in Schedule I or Schedule II; and 1. that has a stimulant, depressant, or hallucinogenic effect on the central nervous system that is substantially similar to or greater than the stimulant, depressant, or hallucinogenic effect on the central nervous system of a controlled dangerous substance described in Schedule I or Schedule II; but 2. (ii) “controlled dangerous substance analogue” does not include: application; or 1. 2. a controlled dangerous substance; a substance for which there is an approved new drug § 506 of the Federal Food, Drug, and Cosmetic Act. 3. a substance exempted for investigational use under - 1 - (2) To the extent intended for human consumption, each controlled dangerous substance analogue is a substance described in Schedule I. (c) The Department may not add a substance to Schedule I under § 5–202 of this title unless the Department finds: (1) a high potential for abuse of the substance; (2) no accepted medical use in the United States for the substance; and (3) a lack of accepted safety for use of the substance under medical supervision.
f37b9e5866d84a0d(a) A person may not distribute Salvia divinorum to an individual under the age of 21 years. (b) In a prosecution for a violation of this section, it is a defense that the defendant examined the purchaser’s or recipient’s driver’s license or other valid identification issued by an employer, a government unit, or an institution of higher education that positively identified the purchaser or recipient as at least 21 years of age. (c) A person who violates this section is guilty of a misdemeanor and on conviction is subject to a fine not exceeding: (1) $1,000 for a first violation; (2) $2,000 for a second violation occurring within 2 years after the first violation; and (3) $6,000 for each subsequent violation occurring within 2 years after the preceding violation. (d) For purposes of this section, each separate incident at a different time and occasion is a separate violation.
876243ddcc4a5561§5–402. (a) Schedule I consists of each: (1) controlled dangerous substance analogue, as defined in subsection (b) of this section; (2) controlled dangerous substance added to Schedule I by the Department under § 5–202(b) of this title; and (3) controlled dangerous substance designated as a Schedule I controlled dangerous substance by the federal government unless the Department objects under § 5–202(f) of this title. (b) (1) In this subsection: (i) “controlled dangerous substance analogue” means a substance: 1. that has a chemical structure substantially similar to the chemical structure of a controlled dangerous substance described in Schedule I or Schedule II; and 2. that has a stimulant, depressant, or hallucinogenic effect on the central nervous system that is substantially similar to or greater than the stimulant, depressant, or hallucinogenic effect on the central nervous system of a controlled dangerous substance described in Schedule I or Schedule II; but (ii) “controlled dangerous substance analogue” does not include: 1. a controlled dangerous substance; 2. a substance for which there is an approved new drug application; or 3. a substance exempted for investigational use under § 506 of the Federal Food, Drug, and Cosmetic Act. (2) To the extent intended for human consumption, each controlled dangerous substance analogue is a substance described in Schedule I. (c) The Department may not add a substance to Schedule I under § 5–202 of this title unless the Department finds: (1) a high potential for abuse of the substance; (2) no accepted medical use in the United States for the substance; and (3) a lack of accepted safety for use of the substance under medical supervision.
787d346d2d75402a(a) Schedule III consists of each controlled dangerous substance by whatever official name, common or usual name, chemical name, or brand name: (1) added to Schedule III by the Department under § 5–202(b) of this title; or (2) designated as a Schedule III controlled dangerous substance by the federal government unless the Department objects under § 5–202(f) of this title. (b) The Department may not add a substance to Schedule III under § 5–202 of this title unless the Department finds: (1) a potential for abuse of the substance that is less than that for the substances listed in Schedule I and Schedule II; (2) well documented and approved medical use of the substance in the United States; and (3) evidence that abuse of the substance may lead to moderate or low physical dependence or high psychological dependence.
2c80653c39676b66§5–708. (a) (1) This section applies to fingernail polish, model airplane glue, or any other substance that causes intoxication, inebriation, excitement, stupefaction, or dulling of the brain or nervous system when smelled or inhaled. (2) This section does not apply to: (i) the inhalation of anaesthesia for medical or dental purposes; or (ii) controlled dangerous substances. (b) (1) A person may not deliberately smell or inhale a substance listed in paragraph (2) of this subsection in an amount that causes intoxication, excitement, stupefaction, or dulling of the brain or nervous system. (2) This section applies to a drug or any other noxious substance or chemical that contains: (i) an aldehyde; (ii) butane; (iii) butyl nitrite; (iv) a chlorinated hydrocarbon; (v) ether; (vi) a fluorinated hydrocarbon; (vii) a ketone; (viii) methyl benzene; (ix) nitrous oxide; (x) an organic acetate; or (xi) another substance containing solvents releasing toxic vapors. (c) A person who violates this section is guilty of a misdemeanor and on conviction is subject to imprisonment not exceeding 6 months or a fine not exceeding $500 or both.
f88515f742a25aa0§5–709. (a) In this section, "distribute" includes actual, constructive, or attempted transfer, exchange, or delivery, regardless of remuneration or agency relationship. (b) A person may not distribute or possess with intent to distribute to another a substance listed in § 5-708 of this subtitle: (1) with the intent to induce unlawful inhaling of the substance; or (2) with the knowledge that the other will unlawfully inhale the substance. (c) A person may not: (1) instruct another in the practice of inhaling or smelling that is prohibited under § 5-708(b) of this subtitle; or (2) distribute a butane canister to a minor. (d) A person who violates this section is guilty of a misdemeanor and on conviction is subject to imprisonment not exceeding 18 months or a fine not exceeding $1,000 or both.
acfde5ec795d04e3(a) Schedule I consists of each: (1) controlled dangerous substance analogue, as defined in subsection (b) of this section; (2) controlled dangerous substance added to Schedule I by the Department under Section 5-202(b) of this title; and (3) controlled dangerous substance designated as a Schedule I controlled dangerous substance by the federal government unless the Department objects under Section 5-202(f) of this title. (b) (1) In this subsection: (i) 'controlled dangerous substance analogue' means a substance: 1. that has a chemical structure substantially similar to the chemical structure of a controlled dangerous substance described in Schedule I or Schedule II; and 2. that has a stimulant, depressant, or hallucinogenic effect on the central nervous system that is substantially similar to or greater than the stimulant, depressant, or hallucinogenic effect on the central nervous system of a controlled dangerous substance described in Schedule I or Schedule II; but (ii) 'controlled dangerous substance analogue' does not include: 1. a controlled dangerous substance; 2. a substance for which there is an approved new drug application; or 3. a substance exempted for investigational use under Section 506 of the Federal Food, Drug, and Cosmetic Act. (2) To the extent intended for human consumption, each controlled dangerous substance analogue is a substance described in Schedule I. (c) The Department may not add a substance to Schedule I under Section 5-202 of this title unless the Department finds: (1) a high potential for abuse of the substance; (2) no accepted medical use in the United States for the substance; and (3) a lack of accepted safety for use of the substance under medical supervision.
44237f42e24a987a(a) A retailer may not distribute, sell, expose for sale, or advertise for sale a tianeptine product to an individual. (b) A retailer that violates subsection (a) of this section is guilty of a misdemeanor and on conviction is subject to a fine not exceeding $5,000, imprisonment for not more than 90 days, or both. (c) In addition to any other penalties under this section, a retailer who violates this section is liable for civil damages sustained by the individual resulting from the violation.
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