Gotta love the blow-off response from my Senator to my letter regarding the flavor ban.
March 19, 2018
Mr. Michael Petro
Martinsville, VA
Dear Mr. Petro:
Thank you for contacting me about regulation of hookah tobacco, cigars, and electronic nicotine delivery systems, which include "e-cigarettes," vaporizers, and vape pens.
In 2016, the U.S. Food and Drug Administration (FDA) issued a final rule that grants the Administration the authority to regulate all tobacco products, including hookah tobacco, cigars, e-cigarettes, and vaporizers. Prior to the announcement of this rule, there was no federal law preventing the sale of these alternative tobacco products to those under the age of eighteen. In reaching this decision, the Center for Tobacco Products considered the scientific and public health case for whether to regulate e-cigarettes as part of its authority under the Federal Food, Drug, and Cosmetic Act. The FDA noted that smoking is the top cause of preventable disease and death in the United States, resulting in 480,000 deaths each year. Decreased rates of traditional cigarette use among youth over the past ten years have been accompanied by significantly higher usage rates of e-cigarettes and other tobacco products. E-cigarette use among high school students has increased by over 900 percent since 2011, with the rate of use rising from 1.5 percent to 16 percent in 2015. Results from a joint study by the FDA and the National Institutes of Health showed that from 2013 to 2014, nearly 80 percent of youth tobacco users reported having used a flavored tobacco product within the past 30 days. The final rule seeks to address these trends through a number of provisions that are designed to restrict youth access to tobacco products, such as requiring age verification by photo ID and prohibiting the distribution of free samples. The FDA has made additional information regarding its regulations available on its website at http://www.fda.gov/TobaccoProducts/Labeling/RulesRegulationsGuidance/ucm394909.htm#rule
On February 16, 2017, Representatives Tom Cole and Sanford Bishop introduced the FDA Deeming Authority Clarification Act of 2017 (H.R. 1136). This legislation would amend the Food, Drug, and Cosmetic Act to change the predicate date for newly deemed tobacco products, instate new licensing and advertising guidelines for vapor products, and require the FDA to develop product standards for vapor product batteries. The House has not yet considered this bill.
While adults may purchase nicotine products if they so choose, the FDA has a legal and public health obligation with respect to young people. I will be sure to keep your views in mind should the Senate consider legislation related to this issue.
Thank you again for contacting me.
Sincerely,
Tim Kaine
March 19, 2018
Mr. Michael Petro
Martinsville, VA
Dear Mr. Petro:
Thank you for contacting me about regulation of hookah tobacco, cigars, and electronic nicotine delivery systems, which include "e-cigarettes," vaporizers, and vape pens.
In 2016, the U.S. Food and Drug Administration (FDA) issued a final rule that grants the Administration the authority to regulate all tobacco products, including hookah tobacco, cigars, e-cigarettes, and vaporizers. Prior to the announcement of this rule, there was no federal law preventing the sale of these alternative tobacco products to those under the age of eighteen. In reaching this decision, the Center for Tobacco Products considered the scientific and public health case for whether to regulate e-cigarettes as part of its authority under the Federal Food, Drug, and Cosmetic Act. The FDA noted that smoking is the top cause of preventable disease and death in the United States, resulting in 480,000 deaths each year. Decreased rates of traditional cigarette use among youth over the past ten years have been accompanied by significantly higher usage rates of e-cigarettes and other tobacco products. E-cigarette use among high school students has increased by over 900 percent since 2011, with the rate of use rising from 1.5 percent to 16 percent in 2015. Results from a joint study by the FDA and the National Institutes of Health showed that from 2013 to 2014, nearly 80 percent of youth tobacco users reported having used a flavored tobacco product within the past 30 days. The final rule seeks to address these trends through a number of provisions that are designed to restrict youth access to tobacco products, such as requiring age verification by photo ID and prohibiting the distribution of free samples. The FDA has made additional information regarding its regulations available on its website at http://www.fda.gov/TobaccoProducts/Labeling/RulesRegulationsGuidance/ucm394909.htm#rule
On February 16, 2017, Representatives Tom Cole and Sanford Bishop introduced the FDA Deeming Authority Clarification Act of 2017 (H.R. 1136). This legislation would amend the Food, Drug, and Cosmetic Act to change the predicate date for newly deemed tobacco products, instate new licensing and advertising guidelines for vapor products, and require the FDA to develop product standards for vapor product batteries. The House has not yet considered this bill.
While adults may purchase nicotine products if they so choose, the FDA has a legal and public health obligation with respect to young people. I will be sure to keep your views in mind should the Senate consider legislation related to this issue.
Thank you again for contacting me.
Sincerely,
Tim Kaine
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