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EDITORIAL |
| FDA legislation |
Correspondence to:
Matthew Myers
National Center for Tobacco-Free Kids, 1707 L Street NW, Suite 800, Washington, DC, 20036, USA; mmyers@TobaccoFreeKids.org
Keywords: FDA legislation
| The first 150 words of the full text of this article appear below. |
In the United States and much of the world cigarettes and other tobacco products remain largely free from meaningful regulation. No national agency currently regulates the manufacture, marketing or sale of tobacco products. The tobacco industry has long taken advantage of the absence of regulation to hide the truth about the health effects of their products; manipulate the levels of toxic constituents and nicotine in its products; deceive consumers about so called reduced risk products; and engage in marketing that is deceptive and appealing to women, youths and vulnerable populations.
For at least the past 15 years there has been a consensus about the need to fill this gap by giving the US Food and Drug Administration authority over tobacco. Recently, the Institute of Medicine of the National Academy of Sciences and the Presidents Cancer Panel of the US National Cancer Institute both concluded that FDA authority is
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