LEGAL STATUS — verified 1 Nov 2026: No temporary Schedule I order for concentrated 7-OH has been published. DEA's 14 Oct 2026 notice of intent would allow an order on or after 13 Nov 2026. MGPI, MGM-15, and MGM-16 remain in Schedule I under the 26 Aug 2026 temporary order. Recheck the Federal Register before counseling.

Public health · legal tracker

Dated status—not legal advice.

Controlled-substance scheduling, food-and-drug enforcement, and retail rules are different mechanisms. Verify the primary source on the day a legal conclusion matters.

Federal wording (verified 1 Nov 2026): No temporary Schedule I order for concentrated 7-OH has been published. DEA’s 14 October 2026 notice of intent (FR 2026-20943) would allow an order on or after 13 November 2026. Correct phrasing is temporary Schedule I action noticed, not yet ordered—not “already federally Schedule I”—until a temporary order appears in the Federal Register. Recheck before counseling.

Federal: concentrated 7-OH

DEA published a 14 October 2026 notice of intent (91 FR 65370, document 2026-20943) to temporarily place 7-hydroxymitragynine and mitragynine pseudoindoxyl (MGPI) in Schedule I when above a specified threshold: greater than 1 mg/g (solids) or 1 mg/mL (liquids), or when the mitragynine-to-(7-OH and/or MGPI) mass ratio is less than 100. The July 2026 notice of intent on 7-OH was withdrawn. The notice states that neither HHS nor DEA has found below-threshold products “safe to use.” Primary sources: GovInfo PDF · Federal Register.

Federal: MGPI, MGM-15, MGM-16

Mitragynine pseudoindoxyl, MGM-15, and MGM-16 have been in Schedule I under a temporary order since 26 August 2026 (a separate FR action). On 14 October 2026 DEA also published companion notice 2026-20942 regarding continued temporary Schedule I placement of MGM-15 and MGM-16. Primary sources: GovInfo PDF · DOJ (9 Oct 2026).

FDA position

FDA states concentrated or enhanced 7-OH products are not approved drugs, lawful dietary ingredients, or authorized food additives, and has recommended scheduling and taken enforcement/seizure actions. Public messaging distinguishes concentrated products from natural leaf while warning about MP and related analogues.

Selected state actions (snapshot)

JurisdictionVerified developmentClinical relevance
California CDPH: kratom- and 7-OH-containing foods/supplements/unapproved drugs illegal to manufacture or sell for consumption; active enforcement/seizures. Food/drug enforcement ≠ blanket Schedule I listing. Retail access can contract before federal scheduling.
Connecticut Guidance reports Schedule I placement of kratom and 7-OH (verify current schedule). State criminal exposure may already differ from federal status.
Florida Emergency Rule 2ER26-1 (effective as verified July 1, 2026) places specified 7-OH-related compounds into Schedule I under rule terms. State exposure while federal temporary orders remain pending.
New York S8925A passed both chambers (June 2026); not shown enacted on bill page at last check—retail threshold proposal. Civil retail prohibition ≠ Schedule I.
Texas Public-health advisory on kratom and concentrated 7-OH. Supports screening and education; not itself scheduling.

Public-health signal

America’s Poison Centers reported 593 7-OH exposure reports in 2025 and 901 in January–June 2026. Among 7-OH-only reports, 38.8% were classified serious, 63.8% treated at a healthcare facility, and 20.5% hospitalized. Surveillance is not incidence—but the direction of travel is clear.

Treatment-capacity concern

Pairing regulation with clinician alerts, naloxone, rapid buprenorphine/methadone access, and surveillance for fentanyl substitution is the public-health point of this resource. See treatment and evidence.

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