FDA Letter API

Fog It Up

Letter data

Company
Fog It Up
Recipient
Fog It Up | United States
Issue date
2018-07-13
Posted date
Not available
FDA office
United States
Subject
Not available
Product
Not available
CMS ID
553051
Reference number
Not available
FEI
Not available
Inspection dates
Not available

Normalized citations

21 CFR: 21-CFR-1140.14(b)(1)

21 U.S.C.: None found

Related FDA links

No related FDA letter link is present in the source index.

Full source text

CLOSEOUT LETTER Fog It Up MARCS-CMS 553051 — July 13, 2018 More Warning Letters Warning Letters About Warning and Close-Out Letters Recipient: Fog It Up United States Issuing Office: United States Center for Tobacco Products 10903 New Hampshire Avenue Silver Spring, MD 20993 July 13, 2018 VIA USPS and Electronic Mail Fog It Up P.O Box 9418 Fountain Valley, CA 92728 admin@fogitup.com RE: Warning Letter issued to Fog It Up (RW1800857) Dear Fog It Up: On May 1, 2018, the United States Food and Drug Administration’s (FDA) Center for Tobacco Products (CTP) issued you a Warning Letter informing you that your V’Nilla Cookies & Milk e-liquid product is misbranded under section 903(a)(1) and/or 903(a)(7)(A) of the Federal Food, Drug, and Cosmetic Act (FD&C Act) because its labeling and/or advertising is false or misleading . The Warning Letter also informed you that this product ismisbranded under section 903(a)(7)(B) because you sold itto a person younger than 18 years of age, in violation of 21 C.F.R. § 1140.14(b)(1). Specifically, FDA determined that the labeling and/or advertising of your V’Nilla Cookies & Milk e-liquid is misleading under section 903(a)(1) and/or 903(a)(7)(A) of the FD&C Act because it causes the product to imitate food products, particularly ones that are marketed toward, and/or appealing to, children. FDA also determined that a person younger than 18 years of age was able to purchase V’Nilla Cookies & Milk e-liquid from your website. Based on our evaluation, it appears that you have taken steps to address the violations identified in the Warning Letter. We note that you may have other tobacco products with labeling and/or advertising that causes the product to be misbranded for similar reasons to those discussed above. You are responsible for taking any necessary actions to bring your tobacco products into compliance with the requirements of the law. This letter does not relieve you or your firm from the responsibility of taking all necessary steps to ensure sustained compliance with the FD&C Act and its implementing regulations or with other relevant legal authority. This letter also will not preclude any regulatory action should violations be observed in the future. Should you have any questions or concerns, please contact me at (301) 796-9235 or by email at elenita.ibarrapratt@fda.hhs.gov . Sincerely, /S/ Ele Ibarra-Pratt Division Director Office of Compliance and Enforcement Center for Tobacco Products VIA Electronic Mail cc: Domains By Proxy, LLC FOGITUP.COM@domainsbyproxy.com GoDaddy.com, LLC abuse@godaddy.com Shopify, Inc. abuse@shopify.com Content current as of: 08/23/2018