Nevada's original whole-kratom Schedule I proposal (R105-26) was withdrawn on June 29, 2026 — but the issue is not over. The Board is expected to return the proposal to a workshop for additional public comment on September 3, 2026.
The Nevada State Board of Pharmacy previously proposed one of the broadest kratom scheduling rules in the country. LCB File R105-26 would have placed whole kratom — not merely concentrated 7-OH products — into Schedule I. That regulatory file was withdrawn by the Board on June 29, 2026.
The withdrawal means R105-26 was not adopted and is no longer an active proposed regulation. Kratom has not been placed into Schedule I under R105-26. However, Board tracking information indicates that the issue is expected to return for additional public comment on September 3, 2026.
The withdrawn regulation went considerably further than scheduling three isolated alkaloids. R105-26 proposed Schedule I control of any material, compound, mixture or preparation containing any quantity of kratom, including natural, synthetic and semisynthetic substances associated with Mitragyna speciosa.
The proposed language specifically included:
The question now isn't whether to support the withdrawn R105-26 file as though it were still pending. The question is what Nevada puts into its replacement proposal.
We are asking the Nevada State Board of Pharmacy to retain the comprehensive approach reflected in R105-26 and recommend Schedule I control that includes:
The current policy debate increasingly attempts to divide the market into supposedly acceptable “natural kratom” and unacceptable concentrated 7-OH products. That distinction does not resolve the underlying regulatory question.
Mitragynine is the principal alkaloid in conventional kratom and is pharmacologically active. Mitragynine is also metabolized in humans to 7-hydroxymitragynine.
Kratom-associated poison-center cases, dependence, withdrawal, adverse events and deaths were documented years before the recent commercial market for concentrated 7-OH products emerged.
Send your comment to the Board's official public comment inbox. It will be logged into the regulatory record.
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This is rulemaking, not legislation. The Board of Pharmacy makes the decision. Legislators are not involved at this stage. Focus your pressure here:
R105-26 may have been withdrawn, but the fight for a whole-kratom Schedule I is not over.
Send your comment now and urge Nevada to close the loopholes.