U.S. House Takes Giant Step Toward Historic Regulation of Tobacc...(dent's Cancer Panel. Tobacco use ...),Health

Tobacco use kills more than 400,000 Americans and costs the nation $96 billion in health care bills each year. Every day, more than 1,000 children become new regular smokers. Yet tobacco products are exempt from the FDA's common-sense regulations that apply to virtually every other product we consume, from food to drugs to cosmetics. This allows tobacco companies to market their deadly and addictive products to children, deceive consumers about the harm their products cause, make changes to their products without disclosing them (such as manipulating nicotine levels in cigarettes), and resist any meaningful change to make their products less harmful.

This legislation would grant the FDA the authority and resources to effectively regulate the manufacturing, marketing and sale of tobacco products. Among other things, it would:

• Restrict tobacco advertising and promotions, especially to children.
• Stop illegal sales of tobacco products to children.
• Require larger, more effective health warnings on tobacco packages and advertising.
• Ban misleading health claims such as "light" and "low-tar" and strictly regulate all health claims about tobacco products to ensure they are scientifically proven and do not discourage current tobacco users from quitting or encourage new users to start.
• Require tobacco companies to disclose the contents of tobacco products, as well as changes in products and research about their health effects.
• Empower the FDA to require changes in tobacco products, such as the removal or reduction of harmful ingredients or the reduction of nicotine levels.
• Fully fund the FDA's new tobacco-related responsibilities with a user fee on tobacco companies so no resources are taken from the FDA's current work.