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Public health groups strongly support bipartisan FDA tobacco legislation

Published on May 20, 2004 at 6:43 PM · No Comments

Statement of American Cancer Society, American Heart Association, American Lung Association and Campaign for Tobacco-Free Kids

Our public health organizations strongly support the bipartisan legislation introduced today in both the House and Senate to provide the U.S. Food and Drug Administration (FDA) with effective authority to regulate tobacco products.  This legislation presents Congress with a truly historic opportunity to protect our children from tobacco addiction and address the number one preventable cause of death in our nation.  We applaud U.S. Senators Mike DeWine (R-OH) and Edward Kennedy (D-MA) and U.S. Representatives Tom Davis (R-VA) and Henry Waxman (D-CA) for their leadership in producing strong bills that put protection of the public health first. We urge both the Senate and the House to quickly enact this legislation into law and to resist all efforts to weaken it.

Every year in America, tobacco use kills more than 400,000 people and costs our nation more than $75 billion in health care bills.  Every day, another 2,000 kids become regular smokers, one-third of whom will die prematurely as a result.  Yet tobacco products are virtually unregulated to protect consumers’ health and safety.  For decades, the tobacco companies have marketed their deadly products to our children, deceived consumers about the harm their products cause, and failed to take any meaningful action to make their products less harmful or less addictive.  The legislation introduced today would finally end the special protection enjoyed by the tobacco industry and protect our children and the nation’s health instead.

This legislation meets the standards long established by the public health community for a strong FDA tobacco regulation bill that protects the public health.  It would give the FDA the necessary tools and resources to effectively regulate the manufacturing, marketing, labeling, distribution and sale of tobacco products.  The FDA would have the authority to:

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