US Congress Proposes Disposable ENDS Product Enforcement Act

Mar.14.2023
US Congress Proposes Disposable ENDS Product Enforcement Act
The Disposable ENDS Product Enforcement Act of 2023 aims to regulate and prioritize enforcement measures against disposable e-cigarettes.

On March 13th, it was reported that the full text of the proposal for the "Disposable ENDS Product Enforcement Act of 2023" has been made public on the official website of the United States Congress. The bill was introduced by Sheila Cherfilus McCormick, a member of the House of Representatives from Florida, and has been assigned to the House Energy and Commerce Committee.


Hillary Schefter-McCormick | Source: Official website of the United States Congress


The bill cites a study released by the U.S. Food and Drug Administration in 2022 that indicates disposable e-cigarettes are the most commonly used type of device among underage individuals in the United States.


Based on this premise, the bill requires that within 90 days of its passage, the Department of Health and Human Services (HHS) must update its enforcement priorities for electronic nicotine delivery systems (ENDS) and other deemed products that have not been authorized for pre-market sale, as outlined in its April 2020 publication. The updated regulations must include measures on how to prioritize enforcement actions against disposable ENDS products, including non-tobacco derived nicotine products.


According to reports, as of March 10, there are four co-sponsors of the bill, all of whom are Democratic members of the House of Representatives, as listed on Congress's website. The House is majority-controlled by Republicans, with 222 seats, while Democrats hold 213 seats. Previously, Republican Kevin McCarthy faced opposition from far-right conservative members before ultimately winning the election as Speaker of the House after 15 rounds of voting, marking the most rounds of voting in a House Speaker election since 1923.


References:


HR901 - One-time Enforcement of ENDS Products Act in 2023.


Additional reading:


A new US bill is pressuring the FDA to crack down on disposable e-cigarettes.


This document has been generated through artificial intelligence translation and is provided solely for the purposes of industry discourse and learning. Please note that the intellectual property rights of the content belong to the original media source or author. Owing to certain limitations in the translation process, there may be discrepancies between the translated text and the original content. We recommend referring to the original source for complete accuracy. In case of any inaccuracies, we invite you to reach out to us with corrections. If you believe any content has infringed upon your rights, please contact us immediately for its removal.

2Firsts Data|China Vape Exports Sink to Three-Year April Low After Tax Rebate Ends, Falling to $694 Million
2Firsts Data|China Vape Exports Sink to Three-Year April Low After Tax Rebate Ends, Falling to $694 Million
China’s e-cigarette export value declined to $694 million in April 2026, marking the lowest April level in the past three years. The data is notable because April was the first full month after China removed export VAT rebates for certain e-cigarette products. Compared with April 2025, export value fell 20.9%; compared with April 2024, it was down 22.3%. Month-on-month, exports dropped 23.2% from March 2026.
Special Report
May.23
Nature Health Comment Urges Wider Role for Smoke-Free Nicotine Products in Tobacco Control
Nature Health Comment Urges Wider Role for Smoke-Free Nicotine Products in Tobacco Control
Ahead of World No Tobacco Day, a Nature Health Comment by Robert Beaglehole, Ruth Bonita and Tikki Pang argues that regulated smoke-free nicotine products could help accelerate the global decline in smoking. The authors propose a “smoke-free 2040” goal and call for risk-proportionate regulation distinguishing cigarettes from lower-risk nicotine alternatives.
News
May.20
BAT Rothmans Upgrades neo™ Boost for glo™ HYPER Series
BAT Rothmans Upgrades neo™ Boost for glo™ HYPER Series
BAT Rothmans said on April 13 that its heated tobacco brand glo™ will launch an upgraded version of neo™ Boost, the dedicated stick for the HYPER series. The company said the refresh focuses on strengthening freshness and cooling sensations to improve the overall user experience.
Apr.14 by 2FIRSTS.ai
FDA Warns Retailers Over Unauthorized Nicotine Pouches Resembling Candy and Everyday Products
FDA Warns Retailers Over Unauthorized Nicotine Pouches Resembling Candy and Everyday Products
The FDA issued warning letters to eight retailers selling unauthorized nicotine pouches and dissolvable tobacco products resembling candy, breath strips and cough drops. The action highlights rising scrutiny of packaging, youth appeal and accidental ingestion risks, as the agency clarifies enforcement priorities for unauthorized ENDS and nicotine pouch products while maintaining PMTA as the legal market pathway.
Special Report
May.21
Thailand’s Bangkok Port Customs Reports E-Cigarette and Nitrous Oxide Seizure Worth More Than THB 27 Million
Thailand’s Bangkok Port Customs Reports E-Cigarette and Nitrous Oxide Seizure Worth More Than THB 27 Million
Bangkok Port Customs on April 28 announced the seizure of 52,000 complete e-cigarettes, 100 gallons of e-liquid and 126,226 canisters of nitrous oxide, with total economic damage exceeding THB 27 million, or about USD 831,178 based on an April 28 USD/THB rate of 32.484. The e-cigarette and e-liquid shipment was valued at THB 5.56 million, or about USD 171,161, while the nitrous oxide shipment was valued at THB 21.27 million, or about USD 654,784.
Apr.29 by 2FIRSTS.ai
Acting CTP Director Says FDA Cut Premarket Tobacco Application Backlog by About 70% Over the Past Year
Acting CTP Director Says FDA Cut Premarket Tobacco Application Backlog by About 70% Over the Past Year
FDA Center for Tobacco Products Acting Director Bret Koplow said at the American Tobacco and Nicotine Forum that the agency has reduced its premarket tobacco application backlog by about 70% over the past year and eliminated the acceptance queue. He said FDA has reviewed about 27 million applications, but only a small number have been authorized, mainly because most submissions lacked the scientific data needed to demonstrate public health benefits.
Apr.23 by 2FIRSTS.ai