Loading…
denverelectroniccigarettes.com was cited for offering electronic nicotine delivery system (ENDS) products for sale without required FDA premarket authorization. The company's website featured tobacco products containing nicotine that failed to comply with Federal Food, Drug, and Cosmetic Act requirements, which mandate premarket authorization for all "new tobacco products" not commercially marketed in the United States before February 15, 2007. The FDA's jurisdiction over these products was clarified under 2022 legislation that extended regulatory authority to products containing nicotine from any source, not just tobacco-derived nicotine.