FDA Grants First PMTA Authorization for Vaping Products in the U.S.
The U.S. Food and Drug Administration (FDA) has for the first time authorized vaping products for legal sale in the U.S. market, allowing RJ Reynolds to sell three Vuse products. Mitch Zeller, director of the FDA’s Center for Tobacco Products, stated that
The U.S. Food and Drug Administration (FDA) has granted the first PMTA authorization for vaping products, allowing RJ Reynolds to sell its three Vuse e-cigarette products. Mitch Zeller, director of the FDA's Center for Tobacco Products, stated in a press release that data from e-cigarette manufacturers indicate that their tobacco-flavored products can benefit addicted adult smokers by reducing exposure to harmful chemicals, potentially allowing them to completely or significantly reduce cigarette consumption. (Associated Press)<\/p>
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