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Policy & Funding· Daily Pulse

DEA Wants to Schedule Concentrated 7-OH Kratom Like Heroin. The Comment Window Closes Today.

The proposed rule targets synthesized, high-concentration kratom shots and gummies — not the leaf tea people have used for years. That distinction is about to get tested at scale.

ByThe Rize NewsroomJuly 31, 20262 min readKratom

Today is the last day to weigh in before the federal government decides how to treat one of the fastest-growing products in the supplement and vape-shop aisle. HHS’s public comment period on DEA’s proposal to temporarily place concentrated 7-hydroxymitragynine — 7-OH, the compound behind the gummies, shots, and dissolvable strips increasingly marketed as “kratom extract” — into Schedule I closes today, July 31. If the comment period doesn’t change DEA’s course, the Attorney General is positioned to issue a formal two-year temporary scheduling order as early as August 5.

The rule is narrower than most of the coverage of it, and that distinction is going to matter to a lot of people who think this is about to make their kratom illegal.

DEA’s proposal targets 7-OH specifically above a defined concentration threshold — 0.050% by dry weight in raw botanical material, or 0.050%/1.00mg in processed extracts and edibles — plus three related synthetic or lab-modified compounds (mitragynine pseudoindoxyl, and two designated only as MGM-15 and MGM-16). It does not touch traditional, low-concentration kratom leaf or tea, the form millions of Americans have used for years to manage chronic pain, opioid withdrawal symptoms, or anxiety without a prescription. HHS and FDA both publicly backed the action, framing it as closing a loophole that let manufacturers chemically concentrate a minor, mildly active compound in raw kratom into something with opioid-like potency and abuse potential — closer, pharmacologically, to a synthetic opioid than to the plant it’s marketed alongside.

That’s a real and defensible distinction on paper. In practice, it’s the kind of line regulators draw that retailers, and the users who’ve come to depend on 7-OH products specifically, don’t always respect at the point of sale. Someone using a high-concentration 7-OH shot to self-manage opioid withdrawal because they can’t access buprenorphine, or because they’re trying to avoid returning to a drug that’s more likely to kill them, is not the same person as someone drinking kratom tea for energy — but both are about to watch the same regulatory hammer fall on very different-looking products sold three feet apart on the same shelf. If the concentrated version disappears from that shelf on August 5 and nothing replaces it for the people actually using it to stay off something stronger, the harm-reduction math on this rule will look very different in six months than it does in the DEA’s press release today.

Sources Cited

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    HHS, FDA Support DEA 7-OH Scheduling ActionU.S. Department of Health and Human Services

Filed Under

policyharm-reductionDrug SchedulingDEAThe Treatment Gap

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