FDA Seeks Nicotine Reduction

This article is from the archive of The New York Sun before the launch of its new website in 2022. The Sun has neither altered nor updated such articles but will seek to correct any errors, mis-categorizations or other problems introduced during transfer.

The New York Sun

The Food and Drug Administration should regulate tobacco and develop a plan to reduce nicotine levels in cigarettes, the Institute of Medicine urged yesterday.

Its report calls on Congress and the president to give FDA the authority to enforce standards for nicotine reduction and to regulate companies’ claims that their products reduce exposure or risk.

“We propose aggressive steps to end the tobacco problem — that is, to reduce tobacco use so substantially that it is no longer a significant public health problem. This report offers a blueprint for putting the nation on a course for achieving that goal over the next two decades,” the director of the Institute of Law, Psychiatry, and Public Policy at the University of Virginia School of Law, Richard Bonnie, said. Mr. Bonnie was chairman of the committee that prepared the report.

“Unfortunately, cigarettes are one of the most dangerous consumer products ever marketed,” Mr. Bonnie said at a briefing.

The report notes that cigarettes are unique in that they contain carcinogens and would be banned under federal law if these statutes did not expressly exempt tobacco.

A bill currently before Congress would give FDA authority to regulate tobacco, but the head of the agency has expressed skepticism. Dr. Andrew von Eschenbach said that if the FDA reduced nicotine levels in cigarettes, people would change their smoking habits to maintain current levels of nicotine.

“We could find ourselves in the conundrum of having made a decision about nicotine only to have made the public health radically worse. And that is not the position FDA is in; we approve products that enhance health, not destroy it,” Dr. von Eschenbach said in an Associated Press interview in March.

Cigarette maker Philip Morris USA has been supporting the legislation that would give FDA power to regulate the industry.

“FDA regulation creates a uniform set of federal standards for the manufacture and marketing of all tobacco products,” the chairman of Philip Morris USA, Michael Szymanczyk, said earlier this year.


The New York Sun

© 2025 The New York Sun Company, LLC. All rights reserved.

Use of this site constitutes acceptance of our Terms of Use and Privacy Policy. The material on this site is protected by copyright law and may not be reproduced, distributed, transmitted, cached or otherwise used.

The New York Sun

Sign in or  Create a free account

or
By continuing you agree to our Privacy Policy and Terms of Use