The enactment of the Family Smoking Prevention and Tobacco Control Act in 2009 gave the US Food and Drug Administration (FDA) authority to regulate tobacco products-specifically, cigarettes, smokeless tobacco, and roll-your-own tobacco products. That authority was extended to all products that contain tobaccoderived substances, including nicotine, in 2016, when the FDA's "Deeming Rule" went into effect, capturing products such as e-cigarettes, cigars, and shisha within the FDA's authority. This chapter focuses on the FDA regulation of e-cigarettes under the Deeming Rule, including the current pre-market authorization requirements that could result in an effective ban on e-cigarettes in the United States.
CITATION STYLE
Chowdhury, A. (2017). Regulation of E-cigarettes in the United States. In Dual Markets: Comparative Approaches to Regulation (pp. 287–302). Springer International Publishing. https://doi.org/10.1007/978-3-319-65361-7_18
Mendeley helps you to discover research relevant for your work.