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Cessation 2024;10(August):35 KEYWORDS TOPICS ABSTRACT In the United States, the Food and Drug Administration (FDA) requires tobacco product manufacturers to submit Premarket Tobacco Product Applications (PMTA) for new products, granting marketing approval only if deemed appropriate for the protection of public health

Given their shared addictive nature, we classify them as substance use

It was that provinces strengthening of its Tobacco Access Act in May 2015 that set the stage for a now Canada-wide ban on flavoured cigarettes

Overall, this represents an exceedingly small share of the overall Shared Savings Program assigned beneficiary population, currently 10.8 million 467 ( beneficiaries

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