ABSTRACT

The FDA has been instrumental in enforcing essential documents and laws related to tobacco product regulations, even though tobacco use is the primary cause of one in five US deaths. The Family Smoking Prevention and Tobacco Control Act passed in 2009, marked the beginning of a comprehensive public health initiative. The FDA has the power to regulate tobacco products, which are the country's highest avoidable cause of death. However, this regulation presents new opportunities and challenges for public health professionals in academia, research, government, and advocacy. On August 23, the FDA released a regulation restricting the sale and distribution of cigarettes and smokeless tobacco products to underage individuals, marking the most extensive program ever implemented to reduce teen tobacco consumption. The FDA's jurisdiction over these products is based on the investigation that led to its assertion of its jurisdiction over these products and the policy considerations that shaped the final rule. Keywords: FDA, Smokeless Tobacco Products, Act, Guidance, Jurisdiction
Publication date: 01/07/2025

https://ijbpas.com/pdf/2025/July/MS_IJBPAS_2025_9230.pdf

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https://doi.org/10.31032/IJBPAS/2025/14.7.9230