FDA WARNING_LETTER - ejuicevapedistro.com - June 10, 2025

On June 6, 2025, the FDA's Center for Tobacco Products issued a Warning Letter to ejuicevapedistro.com after reviewing their website and determining that they offer electronic nicotine delivery system (ENDS) products for sale or distribution in the United States. These products are classified as tobacco products under section 201(rr) of the FD&C Act, as amended on March 15, 2022, to include nicotine from any source.

The FDA identified two specific ENDS products, "Raz DC25000 Disposable Vape - Razzle Dazzle" and "Raz DC25000 Disposable Vape - Strawberry Kiwi Pear," as "new tobacco products" that lack the required premarket authorization order under section 910(c)(1)(A)(i) of the FD&C Act. These products were not commercially marketed in the U.S. as of February 15, 2007, and do not have FDA marketing authorization, nor are they exempt. Consequently, these products are deemed adulterated under section 902(6)(A) and misbranded under section 903(a)(6) of the FD&C Act due to the absence of required information under section 905(j).

The letter states that all new tobacco products marketed without statutory premarket authorization are unlawful and subject to enforcement actions, including civil money