US FDA denies two Vuse menthol e-cig products, cites public health standards

The US Food and Drug Administration (FDA) has denied the premarket tobacco product applications (PMTAs) of two menthol e-cigarette products by RJ Reynolds Vapor Company, following the federal agency’s determination that these products do not meet public health standards.

The agency issued marketing denial orders (MDOs) for Vuse Vibe Tank Menthol 3.0% and the Vuse Ciro Cartridge Menthol 1.5%.

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Antonia Di Lorenzo

Assistant news editor
Antonia is a member of the editorial team and holds a masters degree in Law from the University of Naples Federico II, Italy. She moved in 2013 to London, where she completed a postgraduate course at the London School of Journalism. In the UK, she worked as a news reporter for a financial newswire and a magazine before moving to Barcelona in 2019.

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