On June 22, 2009, President Barack Obama signed into law an Act of Congress which gives the FDA authority to regulate tobacco products. The term “tobacco product” means any product made or derived from tobacco that is intended for human consumption, including any component, part, or accessory of a tobacco product. This includes, among other products, cigarettes, cigarette tobacco, roll-your-own tobacco, and smokeless tobacco.
Currently, there are many "tobacco products" that are not subject to FDA regulation under this Act, such as cigars, pipe tobacco, hookah/shisha, dissolvables, and electronic cigarettes. But the FDA has announced their intention to propose a regulation that would extend the Agency’s authorities to other categories of tobacco products, including electronic cigarettes. The additional tobacco product categories would be subject to general controls, such as registration, product listing, ingredient listing, good manufacturing practice requirements, user fees for certain products, and the adulteration and misbranding provisions, as well as to the premarket review requirements for “new tobacco products” and “modified risk tobacco products.”
Currently, there are many "tobacco products" that are not subject to FDA regulation under this Act, such as cigars, pipe tobacco, hookah/shisha, dissolvables, and electronic cigarettes. But the FDA has announced their intention to propose a regulation that would extend the Agency’s authorities to other categories of tobacco products, including electronic cigarettes. The additional tobacco product categories would be subject to general controls, such as registration, product listing, ingredient listing, good manufacturing practice requirements, user fees for certain products, and the adulteration and misbranding provisions, as well as to the premarket review requirements for “new tobacco products” and “modified risk tobacco products.”