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AgdaPkt 2020-03-09 Joint
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AgdaPkt 2020-03-09 Joint
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Last modified
10/1/2020 11:25:10 AM
Creation date
3/5/2020 4:04:14 PM
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CC Index
CC Index - Document Type
Agenda Packet
Meeting Type
Joint
Agency Type
City Council and Successor Agency and Public Financing Authority
Date
3/9/2020
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9.A. - Page 15 of 31 <br />associated with increased risk of heart attack.10 The American Lung <br />Association has reported that there is risk for irreversible lung damage and <br />disease as a result of vaping.11 <br />(h) The County of San Mateo (the "County") issues permits to tobacco retailers. <br />(Chapter 4.98). In 2018, in order to reduce flavored tobacco product <br />availability, the County adopted Ordinance No. 04799, prohibiting the sale <br />of flavored tobacco products and pharmacy sales of all tobacco products. <br />(i) In spite of these efforts, San Mateo County youth still have access to <br />tobacco products and are using the products. According to the 2018 <br />California Student Tobacco Survey, for Region 20 (San Francisco, San <br />Mateo counties), the current e -cigarette use prevalence among high school <br />students in 2017-2018 was 20.8%. This prevalence is much higher than <br />the state-wide prevalence of 10.9%.12 <br />(j) In June 2009, the Family Smoking Prevention and Tobacco Control Act <br />(Tobacco Control Act) was signed into law to give the U.S. Food & Drug <br />Administration (FDA) authority to regulate the manufacture, distribution, and <br />marketing of tobacco products. The Tobacco Control Act was enacted in <br />order to protect the public and create a healthier future for all Americans.13 <br />(k) A central requirement of the Tobacco Control Act is premarket review of all <br />new tobacco products. Specifically, every "new tobacco product"—defined <br />to include any tobacco product not on the market in the United States as of <br />February 15, 2007—must be authorized by the FDA for sale in the United <br />States before it may enter the marketplace. A new tobacco product may not <br />be marketed until the FDA has found that the product is: (1) appropriate for <br />the protection of the public health upon review of a premarket tobacco <br />application; (2) substantially equivalent to a grandfathered product; or (3) <br />exempt from substantial equivalence requirements. <br />(1) In determining whether the marketing of a tobacco product is appropriate <br />for the protection of the public health, the FDA must consider the risks and <br />benefits of the product to the population as a whole, including users and <br />nonusers of the product, and taking into account the increased or <br />decreased likelihood that existing users of tobacco products will stop using <br />tobacco products and the increased or decreased likelihood that those who <br />do not use tobacco products will start using them. Where there is a lack of <br />° 5 Jun 2019 https://doi.org/10.1161/JAHA.119.012317 Journal of the American Heart Association. 2019;8:e012317 <br />i Moritz, T. (2019, March 18). Vaping: It's All Smoke and Mirrors. Retrieved from https://www.lung.org/about- <br />us/blog/2019/03/vap ing-smoke-and-mirrors.html <br />12 Zhu S -H, Zhuang YL, Braden K, Cole A, Gamst A, Wolfson T, Lee J, Ruiz CG, Cummins SE (2019). Results of the Statewide <br />2017-18 California Student Tobacco Survey. San Diego, California: Center for Research and Intervention in Tobacco Control <br />(CRITC), University of California, San Diego. <br />" FDA. (2018, January 17). Family Smoking Prevention and Tobacco Control Act — An Overview. Retrieved from <br />https://www.fda.gov/tobacco-products/rules-regulations-and-guidance/family-smoking-prevention-and-tobacco-control-act- <br />overview <br />292 <br />
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