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S5383Referred to Committee

End Gas Station Heroin Act

Share:
Introduced
In Committee
3
Passed One Chamber
4
Passed Both
5
Signed into Law
119th
Congress
2026-08-08
Introduced
0
Cosponsors
S
ⓘ
Type

Sponsor

Bernie Moreno
Bernie Moreno
Republican · OH · Senator
Votes with party: 76.0% (885 recorded votes)
Top industries funding sponsor:
  • Conservative Groups$1,210k

Full profile: /officials/M001242

Source: Congress.gov · FEC

Cosponsors (0)

Members who have signed on to support this bill since introduction. Source: Congress.gov.

No cosponsors on record. Bills can pass without cosponsors — this often means the sponsor introduced the bill alone, either because it's a messaging bill, a chairman's mark, or simply early in the legislative cycle.

Latest Action

The most recent step in the bill's legislative path. Committee Activity below shows referrals and reports; the full action-by-action history including floor proceedings lives at Congress.gov →

Read twice and referred to the Committee on the Judiciary.

2026-08-08

Source: Congress.gov

Committee Activity

Currently in

  • Senate Committee on the JudiciaryReferred To · 2026-08-08

Plain-English Summary

Plain-English summary pending. Introduced on 2026-08-08. Check back soon — summaries are generated as bills progress through Congress.

Full Bill Text

Verbatim text published on Congress.gov via GovInfo. Use Cmd+F / Ctrl+F to search within this excerpt.

[Congressional Bills 119th Congress] [From the U.S. Government Publishing Office] [S. 5383 Introduced in Senate (IS)] <DOC> 119th CONGRESS 2d Session S. 5383 To amend the Controlled Substances Act to schedule MGM-15 and MGM-16 as Schedule I Controlled substances, and to amend the controlled Substances Act to schedule synthetic 7-hydroxymitragynine, and Mitragynine Pseudoindoxyl, as a Schedule I above a specific threshold under the Controlled Substances Act, and to expand enforcement actions against drug manufacturers and distributors of emerging synthetic opioids, commonly known as gas station heroin. _______________________________________________________________________ IN THE SENATE OF THE UNITED STATES August 8 (legislative day, August 7), 2026 Mr. Moreno introduced the following bill; which was read twice and referred to the Committee on the Judiciary _______________________________________________________________________ A BILL To amend the Controlled Substances Act to schedule MGM-15 and MGM-16 as Schedule I Controlled substances, and to amend the controlled Substances Act to schedule synthetic 7-hydroxymitragynine, and Mitragynine Pseudoindoxyl, as a Schedule I above a specific threshold under the Controlled Substances Act, and to expand enforcement actions against drug manufacturers and distributors of emerging synthetic opioids, commonly known as gas station heroin. Be it enacted by the Senate and House of Representatives of the United States of America in Congress assembled, SECTION 1. SHORT TITLE. This Act may be cited as the ``End Gas Station Heroin Act''. SEC. 2. SCHEDULING OF 7-HYDROXYMITRAGYNINE AND MITRAGYNINE PSEUDOINDOXYL. Schedule I of section 202(c) of the Controlled Substances Act (21 U.S.C. 812(c)) is amended, in subsection (b), by adding at the end the following: ``(23)(A) 7-hydroxymitragynine (7-OH) and mitragynine pseudoindoxyl, including their salts, isomers, salts of isomers, esters, ethers, and synthetic analogs, whenever the existence of such forms is possible. ``(B) This paragraph shall not apply to 7- hydroxymitragynine or mitragynine pseudoindoxyl naturally occurring in Mitragyna speciosa Korth (kratom) or in a finished kratom product, provided that-- ``(i) in the case of a solid, powdered, or encapsulated product, the concentration of 7- hydroxymitragynine and mitragynine pseudoindoxyl, individually or in combination, does not exceed 1 milligram per gram of product; ``(ii) in the case of a liquid product, the concentration of 7-hydroxymitragynine and mitragynine pseudoindoxyl, individually or in combination, does not exceed 1 milligram per milliliter of product; and ``(iii) the combined amount of 7-hydroxymitragynine and mitragynine pseudoindoxyl, including their salts, isomers, salts of isomers, esters, ethers, and synthetic analogs, does not exceed 1 part per 100 parts mitragynine by mass. ``(C) For purposes of this paragraph, any 7- hydroxymitragynine or mitragynine pseudoindoxyl that is synthesized, chemically converted, concentrated, enriched, isolated, or otherwise produced through manufacturing processes shall not qualify for the exemption described in subparagraph (B).''. SEC. 3. ENFORCEMENT AGAINST EMERGING SYNTHETIC OPIOIDS IN COMMERCIAL DISTRIBUTION. (a) Treatment as a Schedule I Controlled Substance.-- Notwithstanding any other provision of law, a covered emerging synthetic opioid shall, solely for purposes of prohibiting and enforcing against its knowing or intentional manufacture, importation, exportation, distribution, dispensing, or possession with intent to manufacture, import, export, distribute, or dispense, be treated as a controlled substance in Schedule I of section 202(c) of the Controlled Substances Act (21 U.S.C. 812(c)). (b) Civil and Criminal Enforcement.--No person shall be subject under this section to criminal or civil enforcement based solely on the purchase, receipt, simple possession, or personal use of a covered emerging synthetic opioid. (c) Covered Emerging Synthetic Opioid.--For purposes of this section, the term ``covered emerging synthetic opioid'' means a substance that-- (1) is being manufactured, offered, advertised, sold, distributed, or otherwise introduced into commercial distribution, or is intended by the person engaging in the prohibited conduct to be introduced into commercial distribution; (2) is an…
Show the remaining 604 wordsHide the remaining 604 words
opioid receptor agonist, or partial agonist and, based on scientifically reliable evidence, demonstrates greater functional potency than morphine at the human mu-opioid receptor in a validated assay identified by regulation, or demonstrates greater analgesic or respiratory-depressant potency than morphine based on other scientifically reliable evidence; (3) is produced through chemical synthesis or semisynthesis; (4) is not the subject of an approved application under section 505 of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 355); (5) is intended for human consumption; (6) is not otherwise listed in any schedule under section 202 of the Controlled Substances Act (21 U.S.C. 812); and (7) is not excluded under subsection (g). (d) Covered Conduct.--This section shall apply only to the knowing or intentional manufacture, distribution, or possession with intent to manufacture or distribute a covered emerging synthetic opioid. (e) No Simple Possession Enforcement.--No person may be investigated, arrested, charged, prosecuted, or subjected to civil penalties under this section solely for simple possession or personal consumption of a covered emerging synthetic opioid. Nothing in this subsection shall prohibit enforcement based on possession with intent to manufacture, distribute, dispense, import, or export. (f) Relationship to the Controlled Substance Analogue Enforcement Act.--If a substance qualifies both as-- (1) a controlled substance analogue under section 102(32) of the Controlled Substances Act (21 U.S.C. 802(32)); and (2) a covered emerging synthetic opioid under this section, the Attorney General may proceed under section 203 of the Controlled Substances Act (21 U.S.C. 813), this section, or any other applicable provision of Federal law. Nothing in this section shall expand or limit the authority of a State attorney general or other State official under State law. (g) Exclusions.--The term ``covered emerging synthetic opioid'' does not include-- (1) a substance approved as a drug for medical treatment under the Controlled Substances Act (21 U.S.C. 801 et seq.); (2) a substance not intended for human consumption; (3) a naturally occurring constituent of a plant, fungus, or other botanical material, or a constituent derived through brewing or extraction process of a natural plant, fungus, or other botanical material, unless the constituent has been intentionally, isolated, enriched, concentrated, chemically converted, or added to a product for human consumption; (4) a substance possessed or transferred solely for legitimate scientific, medical, forensic, analytical, or law- enforcement purposes; or (5) a substance otherwise exempted by the Attorney General through regulation. (h) Limitation to Commercial Conduct.--Enforcement under this section may be based only on the quantity or portion of a substance that is-- (1) introduced or intended to be introduced into commercial distribution; and (2) connected to conduct described in subsection (a). The presence of the same substance outside commercial distribution, including possession for authorized research, analytical testing, forensic examination, or other noncommercial purposes, shall not independently subject that substance or conduct to enforcement under this section. (i) Definitions.--For the purposes of this section-- (1) the term ``commercial distribution'' means the advertisement, offering for sale, sale, shipment, transfer for value, or distribution of a substance or product in or affecting interstate, intrastate, or foreign commerce; (2) whether a substance is ``intended for human consumption'' shall be determined from all relevant facts and circumstances, potentially including labeling, advertising, dosage form, method of sale, representations by the seller, customary use, and evidence concerning the intended market; (3) the term ``scientifically reliable evidence'' includes validated in vitro, animal, human, pharmacokinetic, pharmacodynamic, receptor-binding, functional-activity, or other scientifically accepted evidence identified by the Attorney General, in consultation with the Secretary of Health and Human Services; and (4) the term ``semisynthesis'' means the chemical modification or conversion of a naturally occurring substance into a chemically distinct substance. <all>
Open clean-text viewRead on Congress.gov →

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