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The applications for these products did not present sufficient scientific evidence to show that the potential benefit to adult smokers outweighs the risks of youth initiation and use. After reviewing the premarket tobacco product applications (PMTA) for the menthol products, the FDA determined they lacked sufficient evidence to demonstrate that permitting the marketing of the products would be appropriate for the protection of the public health, the standard used to judge applications required by the 2009 Family Smoking Prevention and Tobacco Control Act

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