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  5. VR Products I LLC d/b/a eJuiceDB - 665291 - 08/23/2023
  1. Warning Letters

WARNING LETTER

VR Products I LLC d/b/a eJuiceDB MARCS-CMS 665291 —

Delivery Method:
VIA UPS and Electronic Mail
Reference #:
RW2301996
Product:
Tobacco
Recipient:
Recipient Name
Scott Silverman
VR Products I LLC d/b/a eJuiceDB

591 Stewart Ave Ste 520
Garden City, NY 11530-4779
United States

info@ejuicedb.com
info@ecvd.co
Issuing Office:
Center for Tobacco Products

United States

August 23, 2023

WARNING LETTER

Dear Scott Silverman:

The Center for Tobacco Products of the U.S. Food and Drug Administration (FDA) recently reviewed the website https://www.ejuicedb.com and determined that electronic nicotine delivery system (ENDS) and e-liquid products listed there are offered for sale or distribution to customers in the United States.

Under section 201(rr) of the Federal Food, Drug, and Cosmetic Act (FD&C Act) (21 U.S.C. § 321(rr)), these products are tobacco products because they are made or derived from tobacco or contain nicotine from any source, and are intended for human consumption. Certain tobacco products, including ENDS products, are subject to FDA jurisdiction under section 901(b) of the FD&C Act (21 U.S.C. § 387a(b)) and 21 C.F.R. § 1100.1, and are required to be in compliance with the requirements in the FD&C Act.

Please be aware that on March 15, 2022, the President signed legislation to amend the FD&C Act to extend FDA’s jurisdiction to products “containing nicotine from any source,” not just nicotine derived from tobacco. See Consolidated Appropriations Act, 2022, Public Law 117-103, Division P, Title I, Subtitle B. Specifically, this legislation expanded the definition of “tobacco product” under section 201(rr) of the FD&C Act (21 U.S.C. § 321(rr)) to include products containing nicotine from any source. Tobacco products, including ENDS products, containing nicotine from any source, must be in compliance with the FD&C Act and its implementing regulations. For more information, please see https://www.fda.gov/tobacco-products/ctp-newsroom/requirements-products-made-non-tobacco-nicotine-take-effect-april-14.

Generally, to be legally marketed in the United States, the FD&C Act requires “new tobacco products” to have a premarket authorization order in effect. A “new tobacco product” is any tobacco product that was not commercially marketed in the United States as of February 15, 2007, or any modified tobacco product that was commercially marketed after February 15, 2007 (section 910(a) of the FD&C Act; 21 U.S.C. § 387j(a)). Generally, a marketing authorization order under section 910(c)(1)(A)(i) of the FD&C Act (21 U.S.C. § 387j(c)(1)(A)(i)) is required for a new tobacco product unless (1) the manufacturer of the product submitted a report under section 905(j) of the FD&C Act (21 U.S.C. § 387e(j)) and FDA issues an order finding the product substantially equivalent to a predicate tobacco product (section 910(a)(2)(A) of the FD&C Act) or (2) the manufacturer submitted a report under section 905(j)(1)(A)(ii) of the FD&C Act (21 U.S.C. § 387e(j)(1)(A)(ii)) and all modifications are covered by exemptions from the requirements of substantial equivalence granted by FDA under section 905(j)(3) of the FD&C Act (21 U.S.C. § 387e(j)(3)).

New Tobacco Products Without Required Marketing Authorization are Adulterated and Misbranded

Our review of the website https://www.ejuicedb.com revealed that you offer for sale or distribution to customers in the United States the following ENDS and e-liquid products that lack a marketing authorization order, including: Snowwolf Ease Disposable Vape – 8000 Puffs, Blue Cotton Candy; Straw 3000 Sips Disposable Vape Pen – 3000 Puffs, Spryte; Pod Mesh FLO 4000 Disposable Vape Pen – 4000 Puffs, Lemon Sugar Cookie; Glamee Dice 6000 Disposable Vape Pen – 6000 Puffs, Bubble Gum; Lost Mary Elf Bar OS5000 Disposable Vape – 5000 Puffs, Cherry Cola; Esco Bars Mesh Rainbow Disposable Vape – 2500 Puffs; Esco Bars Kilo Disposable Vape Pen – 4000 Puffs, Brazzberry; Cracked Berries and Milk by Lady Boss Vapor E-Liquid; Elf Bar TE5000 Disposable Vape – 5000 Puffs, Juicy Peach; Elf Bar Funky Republic Ti7000 Disposable Vape – 7000 Puffs, Pink Bomb; and Elf Bar BC5000 Disposable Vape – 5000 Puffs, Cherry Lemon Mint. These products do not have a marketing authorization order.

These ENDS and e-liquid products are new tobacco products because they were not commercially marketed in the United States as of February 15, 2007. These products do not have an FDA marketing authorization order in effect under section 910(c)(1)(A)(i) of the FD&C Act and are not otherwise exempt from the marketing authorization requirement. Therefore, these products are adulterated under section 902(6)(A) of the FD&C Act. In addition, these products are misbranded under section 903(a)(6) of the FD&C Act because a notice or other information respecting these products was not provided as required by section 905(j) of the FD&C Act.

Additional Considerations

FDA finds these products particularly concerning because the product labeling and/or advertising for the Snowwolf Ease, Straw 3000 Sips ENDS, Pod Mesh FLO 4000, and Glamee Dice 6000 products (see Exhibits A) are likely to promote use of the products by youth by imitating beverage containers and children’s toys (see Exhibits B). Further, the products’ design is likely to promote the use of the products by youth because they help conceal the nature of the product as a tobacco product from parents, teachers, or other adults, and therefore could be openly carried without revealing to parents, teachers, or other adults that the products are tobacco products. FDA is concerned about the rising youth appeal and dramatic rise in youth use of ENDS products. Any efforts to entice youth to use tobacco products are of concern to FDA. Sales of such unauthorized tobacco products are prohibited, and FDA is concerned that your actions likely encourage unlawful sales, maintain or increase youth use, and contribute to the public health and safety concerns associated with ENDS products.

Snowwolf Drink
Green Tumbler
Blue Soda

 

Stackable Dice

Conclusion and Requested Actions

FDA has determined that your firm markets new tobacco products lacking premarket authorization in the United States. All new tobacco products on the market without the statutorily required premarket authorization are marketed unlawfully and are subject to enforcement action at FDA’s discretion.

For a list of products that received marketing granted orders, please visit our website: https://www.fda.gov/tobacco-products/market-and-distribute-tobacco-product/tobacco-products-marketing-orders#PMTAView%20all%20marketing%20granted.

The violations discussed in this letter do not necessarily constitute an exhaustive list. You should address any violations that are referenced above, as well as violations that are the same as or similar to those stated above, and promptly take any necessary actions to bring the tobacco products you offer for sale or distribution in the United States into compliance with the FD&C Act. It is your responsibility to ensure that these tobacco products and all related labeling and/or advertising on this website, on any other websites (including e-commerce, social networking, or search engine websites), in any other media in which you advertise, and in any retail establishments comply with each applicable provision of the FD&C Act and FDA’s implementing regulations. Failure to address any violations of the FD&C Act, 21 U.S.C. § 301 et seq., and implementing regulations relating to tobacco products including the tobacco regulations in 21 C.F.R. Parts 1140, 1141, and 1143, may lead to regulatory or legal action, including, but not limited to, civil money penalties, seizure, and/or injunction. However, this Warning Letter does not constitute “written notice” for purposes of section 303(f)(9)(B)(i)(II) of the FD&C Act. Please note that tobacco products offered for import into the United States that appear to be adulterated or misbranded may be detained or refused admission.

Please submit a written response to this letter within 15 working days from the date of receipt describing your actions to address any violations and bring these products into compliance, including the dates on which you discontinued the violative sale and/or distribution of these tobacco products and your plan for maintaining compliance with the FD&C Act. If you believe that these products are not in violation of the FD&C Act, include your reasoning and any supporting information for our consideration. This letter notifies you of our findings and provides you with an opportunity to address them. You can find the FD&C Act through links on FDA’s homepage at http://www.fda.gov.

Please note your reference number, RW2301996, in your response and direct your response via email at CTPCompliance@fda.hhs.gov and to the following address:

DPAL-WL Response, Office of Compliance and Enforcement
FDA Center for Tobacco Products
c/o Document Control Center
Building 71, Room G335
10903 New Hampshire Avenue
Silver Spring, MD 20993-0002

If you have any questions about the content of this letter, please contact Bryan Hills at (301) 796-9367 or via email at CTPCompliance@fda.hhs.gov.

Sincerely,
/S/

Ann Simoneau, J.D.
Director
Office of Compliance and Enforcement
Center for Tobacco Products

VIA UPS, USPS, and Electronic Mail

cc:

VR Products I, LLC
Attn: Scott Silverman
40 Melville Road Melville, NY 11747-3173
info@VapeRanger.com

VR Products I, LLC
Attn: Scott Silverman
PO Box 106
Old Westbury, NY 11568

GoDaddy.com, LLC
abuse@godaddy.com

Shopify, Inc.
abuse@shopify.com

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