Page:United States Statutes at Large Volume 123.djvu/1811

 123STA T . 1 79 1 PUBLIC LA W 111 – 31 —J U NE 22, 2 0 09 (includ in gsmoke cons t ituents ), ing r edients, com p onents, a nd additi v es .‘ ‘( 2 ) A n y or all documents (including underlying scienti f ic information) relating to researc h activities, and research findings, conducted, supported, or possessed b y the manufac - turer (or agents thereof) that relate to the issue of w hether a reduction in risk to health from tobacco products can occur upon the employment of technology available or known to the manufacturer. ‘‘( 3 ) Any or all documents (including underlying scientific or financial information) relating to marketing research involving the use of tobacco products or marketing practices and the effectiveness of such practices used by tobacco manufac- turers and distributors. An importer of a tobacco product not manufactured in the U nited S tates shall supply the information re q uired of a tobacco product manufacturer under this subsection. ‘‘(c) TIMEFOR S UB MI S SIO N . — ‘‘( 1 ) I N G ENER AL .—At least 90 days prior to the delivery for introduction into interstate commerce of a tobacco product not on the market on the date of enactment of the F amily Smoking P revention and Tobacco C ontrol Act, the manufacturer of such product shall provide the information required under subsection (a). ‘‘(2) D IS C LOSURE OF A D DI T I V E.—If at any time a tobacco product manufacturer adds to its tobacco products a new tobacco additive or increases the quantity of an e x isting tobacco additive, the manufacturer shall, except as provided in para- graph (3), at least 90 days prior to such action so advise the Secretary in writing. ‘‘(3) DISCLOSURE OF OT H ER ACTIONS.—If at any time a tobacco product manufacturer eliminates or decreases an existing additive, or adds or increases an additive that has by regulation been designated by the Secretary as an additive that is not a human or animal carcinogen, or otherwise harmful to health under intended conditions of use, the manufacturer shall within 6 0 days of such action so advise the Secretary in writing. ‘‘(d) DATA L IST.— ‘‘(1) IN GENERAL.— N ot later than 3 years after the date of enactment of the Family Smoking Prevention and Tobacco Control Act, and annually thereafter, the Secretary shall pub- lish in a format that is understandable and not misleading to a lay person, and place on public display (in a manner determined by the Secretary) the list established under sub- section (e). ‘‘(2) CONSUMER RESEARCH.—The Secretary shall conduct periodic consumer research to ensure that the list published under paragraph (1) is not misleading to lay persons. Not later than 5 years after the date of enactment of the Family Smoking Prevention and Tobacco Control Act, the Secretary shall submit to the appropriate committees of Congress a report on the results of such research, together with recommendations on whether such publication should be continued or modified. ‘‘(e) DATA COLLECTION.—Not later than 2 4 months after the date of enactment of the Family Smoking Prevention and Tobacco Control Act, the Secretary shall establish, and periodically revise Deadlin e . Deadline. R e ports . Re c o m menda - tions. Deadlines. Pub lication. Public in f ormation.