A regulatory look at nicotine analogues in the US market

Vaping and oral snuff products containing synthetic nicotine analogues have been found in the US marketplace this year. These products are promoted as exempt from the US Food and Drug Administration (FDA) premarket tobacco product application (PMTA) process and avoid federal and state regulations.

This report explains what nicotine analogues are and what their current US federal legal status is, looks at criticism for the FDA’s lack of regulations on them, and predicts the future of these compounds in the country.

 

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Kristina Iashina

Junior legal analyst
Kristina holds a Masters Degree in International Law from Moscow State Linguistic University, Russia. In 2020 she completed a six-month exchange programme at the University of Malaga. She has worked as a legal secretary at the Ninth Arbitration Court of Appeal, Russia; and as a legal assistant in a law firm in Moscow.

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