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Smoking and health-related quality of life among Korean adults

FDA would have broad authority to promulgate tobacco product standards whenever such a standard is found to be appropriate for protection of the public health, taking into consideration the risks and benefits to the population as a whole, including users and non-users of tobacco products. (The bill embodies the principles relating to products purporting to reduce exposure to toxins and to reduce disease risk developed by the IOM in Clearing the Smoke [2001].) Legally required package warnings would be strengthened immediately and FDA would have the authority to revise these requirements upon finding that such a change would promote greater public understanding of the risks associated with tobacco. FDA would have authority to restrict the sale and distribution of a tobacco product if the Secretary [of the U.S

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