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WARNING LETTER
•Sunshine Vape

Sunshine Vape – FDA Warning Letter

Record Details

The FDA Center for Tobacco Products issued a Warning Letter to Keith Cohen-Skali regarding e-liquid products sold on sunshinevape.com. An FDA review determined that Sunshine Vape Cowboy e-liquid, classified as a tobacco product under section 201(rr) of the FD&C Act, was sold to a person younger than 18 years of age. This sale constitutes a violation of 21 C.F.R. § 1140.14(b), which prohibits retailers from selling covered tobacco products to minors. Consequently, the product is deemed misbranded under section 903(a)(7)(B) of the FD&C Act. The letter emphasizes that this violation is not exhaustive and requires immediate correction of the identified issue and similar deficiencies to ensure full compliance with the FD&C Act and FDA regulations across all sales and advertising platforms. The firm must submit a written response within 15 working days detailing corrective actions, including dates of discontinuing violative sales and a plan for sustained compliance. Failure to comply could lead to severe FDA enforcement actions, such as civil money penalties, no-tobacco-sale orders, criminal prosecution, seizure, injunction, or detention of imported products.

Company
Sunshine Vape
Product type
Tobacco
Office
Center for Tobacco Products
People
  • Ann Simoneau (Director)
  • Keith Cohen-Skali
View Company Profile

ID · 77cf3241-a424-4e9e-b76a-537fe9228054

Violation Codes5
21 U.S.C. 321(rr)21 U.S.C. 387a(b)21 U.S.C. 387c(a)(7)(B)21 CFR 1140.14(b)21 CFR 1100.2

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