The Destruction of CDC’s Office on Smoking and Health Is a Major Setback for Public Health
The CDC’s Office on Smoking and Health (OSH) has played a large role in the progress the country has made toward reducing cigarette smoking rates to near-record lows in the U.S. and stopping the worst of the impacts of the youth vaping epidemic that was ignited by the e-cigarette company Juul. OSH is responsible for the Tips from Former Smokers media campaign, which helped over one million people quit smoking in its first six years on the air6, as well as other activities that significantly contributed to reductions in tobacco use:
- Providing grants to all 50 states, the District of Columbia and U.S. territories to aid in state and local efforts to reduce tobacco use as part of its National Tobacco Control Program;
- Establishing best practices for running tobacco prevention and control programs and providing technical assistance and expertise to states;
- Ensuring that the country had an accurate picture of how many people in the U.S. used tobacco products by coordinating a comprehensive tobacco use surveillance system to collect information on adult and youth tobacco use as well as exposure to secondhand smoke;
- Helping to write Surgeon General’s reports on tobacco use and otherwise contribute to and synthesize scientific findings on tobacco use and exposure to secondhand smoke.
The dismantling of OSH is devastating for public health. No other agency or organization inside or outside the federal government will be able to fully fill this void. Unless reversed, this will degrade the country’s efforts to fight tobacco use and lead to a resurgence of tobacco use in the U.S.
FDA Center for Tobacco Products Shifts Focus to Authorizing New Products with Seemingly Little Regard for Impact on Kids
Throughout 2025, FDA’s Center for Tobacco Products (CTP) allowed new tobacco products on the market and granted more modified risk or modified exposure orders for tobacco products. They issued marketing granted orders for multiple new e-cigarette products, including several brands of menthol e-cigarettes and 20 Zyn nicotine pouch products, many of which were flavored products. Then, CTP announced an accelerated review process for premarket tobacco applications for nicotine pouches with almost no details about how the process will work. Finally, they seem poised to continue a modified exposure order for the IQOS heated tobacco product, and they scheduled an initial meeting of the Tobacco Products Scientific Advisory Committee for January 22, 2026, for a modified risk tobacco product application for many types of Zyn nicotine pouches.
Prior to 2025, CTP had only authorized one type of menthol flavored e-cigarette for sale, demonstrating how much has changed in the course of a year. The tobacco industry has already noticed this shift and more applications for new tobacco products and modified risk orders will likely be forthcoming in 2026. Recent decisions seem to have ignored the potential impact on kids from authorizing these new tobacco products, particularly flavored products. This is especially true of nicotine pouches given the increasing use by kids seen in the 2025 Monitoring the Future Survey released in December 20257.
The Lung Association will continue to advocate for FDA to follow the public health standard in the Tobacco Control Act and still maintains that flavored tobacco products should not be able to meet that standard given the impact on youth use.
To help address the continuing youth e-cigarette epidemic, the American Lung Association and the Ad Council launched the #DoTheVapeTalk youth vaping awareness campaign to provide parents with the facts to address the dangers of vaping with their kids, while they’re still willing to listen.
Congress Places Requirements on and Gives Additional Authorities to FDA Center for Tobacco Products in FY2026 Budget; Yet to Act on E-Cigarette User Fees
In November 2025, as part of the legislation that ended the 43-day government shutdown, Congress passed, and President Trump signed into law, the fiscal year 2026 Agriculture-FDA bill that includes funding for FDA’s CTP. The bill maintains level funding for CTP through September 30, 2026, but for the first time places requirements on how CTP must spend the funds. CTP is required to spend not less than $200 million in enforcement against illicit e-cigarettes, including at least $2 million to support the federal multi-agency taskforce created in 2024. The bill also granted CTP destruction authority for illegal tobacco products seized at the border, allowing them to be disposed of rather than returned. FDA possesses similar authority for drugs and devices, and this authority will hopefully serve as an additional disincentive to illegal sales.
One related issue that Congress has yet to act on is giving CTP the authority to collect user fees on e-cigarettes. CTP currently collects $712 million in user fees from tobacco products; however, due to provisions in the Tobacco Control Act, cannot collect such user fees from e-cigarettes. Given the new Congressional requirements in the fiscal year 2026 budget involving enforcement against illicit e-cigarettes, now would be the perfect time for Congress to allow FDA to collect these user fees.
H.R. 1 Threatens Access to Tobacco Cessation Treatment; Future Independence of U.S. Preventive Services Task Force in Doubt
Over the past 13 years, access to tobacco cessation treatment has increased due to expansion of state Medicaid programs and the availability of healthcare coverage through the Affordable Care Act (ACA). Unfortunately, in July 2025, Congress passed legislation with devastating cuts to healthcare coverage, thereby impacting access to tobacco cessation treatment. The Congressional Budget Office (CBO) estimates that 10 million people will lose their healthcare coverage as a result of H.R. 18. Congress also failed – in H.R. 1 and other legislation throughout the year – to extend enhanced healthcare tax credits that help millions of people afford quality, affordable coverage through the ACA marketplace. This will result in an additional four million people losing coverage, with premiums skyrocketing for millions more.
The Supreme Court upheld the ACA’s requirement that most insurers cover any service that receives an A or B from the United States Preventive Services Task Force (USPSTF) without cost sharing in the Braidwood case. However, the Court also reaffirmed that the Secretary of Health and Human Services has the authority to accept or deny any recommendations received, and to appoint, supervise and remove USPSTF members, leaving open the possibility of future changes to preventive services by the Secretary. Press reports during 2025 speculated that the current members of USPSTF would be replaced9, but that had not occurred at the time the content for this report was finalized. Tobacco cessation currently has an A grade from USPSTF.
Graphic Cigarette Warning Labels Delayed Indefinitely; FDA Proposes Rule to Reduce Nicotine Levels in Cigarettes and Some Other Tobacco Products
Congress required FDA to implement graphic warning labels on cigarettes as part of the Tobacco Control Act over 15 years ago. In November 2024, after the U.S. Supreme Court declined to hear an appeal of an earlier Fifth Circuit Court of Appeals decision that upheld FDA’s graphic warning labels on cigarettes on constitutional grounds, it seemed likely that the warning labels might finally become a reality.
However, graphic cigarette warning labels now look far less likely to move forward, with two adverse decisions by District Court judges in the 5th and 11th Circuit on different procedural grounds in 2025. The decision in the 5th Circuit in a lawsuit filed by the tobacco company Reynolds American was based on FDA putting forward a different number of warnings in its final graphic cigarette warning rule (11) than outlined in the Tobacco Control Act (9). The decision in the 11th Circuit in a case filed by the tobacco company Altria was based on FDA not providing the raw data in the studies used to support the graphic cigarette warnings rule to the tobacco company plaintiffs. The Department of Justice has appealed both decisions to the 5th and 11th Circuit Court of Appeals, but no decisions had been issued in either case when the content for this report was finalized.
In January 2025, FDA issued a proposed rule to reduce nicotine levels in cigarettes and some other combusted tobacco products. The Lung Association appreciates FDA proposing this rule; reducing nicotine levels in tobacco products to nonaddictive levels could prevent many youth from becoming addicted and make it easier for tobacco users to quit. In September 2025, the Lung Association filed comments supporting the rule with 76 other public health, medical and civil rights organizations, as well as additional comments with the American Academy of Pediatrics and the American Thoracic Society calling for the rule to be expanded to include all tobacco products, including e-cigarettes and nicotine pouches. We do not anticipate action on the proposed rule in the next few years.