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  5. ACH Group, LLC d/b/a Candy Co E-Liquids - 552811 - 05/01/2018
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CLOSEOUT LETTER

ACH Group, LLC d/b/a Candy Co E-Liquids MARCS-CMS 552811 —


Recipient:
Recipient Name
Allen Park
ACH Group, LLC d/b/a Candy Co E-Liquids

14946 Shoemaker Ave Ste A
Santa Fe Springs, CA 90670
United States

Issuing Office:
Center for Tobacco Products

United States


 HHS logo                                   HHS logo

DEPARTMENT OF HEALTH 
AND HUMAN SERVICES
FOOD AND DRUG ADMINISTRATION
SILVER SPRING, MD 20993
UNITED STATES OF AMERICA
FEDERAL TRADE COMMISSION
BUREAU OF CONSUMER PROTECTION
WASHINGTON, D.C. 20580

 

May 1, 2018
 
VIA UPS and Electronic Mail
 
Allen Park
ACH Group, LLC d/b/a Candy Co E-Liquids
14946 Shoemaker Ave Ste A
Santa Fe Springs, CA 90670
candycoeliquids@gmail.com
sales@candycoeliquids.com 
 
WARNING LETTER
 
Dear Allen Park:
 
This is to advise you that the Center for Tobacco Products of the U.S. Food and Drug Administration (FDA) and the U.S. Federal Trade Commission (FTC) recently reviewed the website http://www.candycoeliquids.com from which you take orders for Patches by Candy Co. e-liquid. FDA has determined that the e-liquid products listed there are manufactured and 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)), as amended by the Family Smoking Prevention and Tobacco Control Act, these products are tobacco products because they are made or derived from tobacco and intended for human consumption. Certain tobacco products, including e-liquids, are subject to FDA jurisdiction under section 901(b) of the FD&C Act (21 U.S.C. § 387a(b)). In addition, the FTC has reviewed your marketing for Patches by Candy Co. e-liquid under Section 5 of the FTC Act, 15 U.S.C. § 45(a).
           
FD&C Act Misbranding Violation
 
FDA has determined that your Patches by Candy Co. e-liquid is misbranded under section 903(a)(1) of the FD&C Act (21 U.S.C. § 387c(a)(1)) and/or section 903(a)(7)(A) of the FD&C Act (21 U.S.C. § 387c(a)(7)(A)) because its labeling and/or advertising is false or misleading.
 
FDA’s investigation of the website http://www.candycoeliquids.com revealed it sells or distributes Patches by Candy Co. e-liquid with labeling and/or advertising that causes it to imitate food products, particularly ones that are marketed toward, and/or appealing to, children (see Exhibit A). Specifically, the labeling and/or advertising of the product looks very similar to candy that is primarily marketed toward, or appealing to, children, such as Sour Patch Kids or other candies that are coated in sugar and/or are in the shape of bottles (see Exhibit B). For example, the labeling and/or advertising for Patches by Candy Co. e-liquid includes the terms “Candy” and “Patches,” as well as images of yellow, red, green, orange, and blue bottles coated in a sugar-like substance prominently placed on the front of the packaging. These same bottles also appear to be emerging from the top of the packaging, as if to indicate that these sugar coated, brightly colored items are inside. Additionally, the labeling and/or advertising contains a label on the back that is substantially similar to a food Nutrition Facts label. Further, your website describes the product as “[a]n utterly delicious, sour coated, sweet centered jelly candy.” This labeling and/or advertising causes the product to imitate candy, particularly one that is marketed toward, and/or appealing to, children and is therefore misleading.
 
Tiny Candy 
 
Children are at particular risk for ingesting e-liquid products with labeling and/or advertising that causes the product to imitate a food or beverage, particularly a food or beverage that is typically marketed toward, and/or appealing to, children. Moreover, children are at particular risk because exposure to the nicotine in the e-liquid product, even in relatively small amounts, could result in acute toxicity. Child poisonings due to the ingestion of liquid nicotine have recently increased substantially.  Severe harms can occur in small children from ingestion of liquid nicotine, including death from cardiac arrest, as well as seizure, coma, and respiratory arrest.
 
Given that the labeling and/or advertising on Patches by Candy Co. e-liquid describes its nicotine content as high as 12mg/mL, with a total volume of 60mL, an accidental ingestion of about a quarter of a teaspoon would reach the lower end of the fatal dose range for an average two-year-old. Additionally, an accidental ingestion of approximately 1% of a teaspoon would reach the lower end of the non-fatal acute toxicity range for an average two-year-old.
 
The FD&C Act provides, in part, that a tobacco product shall be deemed to be misbranded (1) if its labeling is false or misleading in any particular (section 903(a)(1)), or (2) if the tobacco product is distributed or offered for sale in any State and its advertising is false or misleading in any particular (section 903(a)(7)(A)).  The labeling and/or advertising for Patches by Candy Co. e-liquid is misleading because it causes the product to imitate candy, particularly one that is marketed toward, and/or appealing to, children.  Therefore, the product is misbranded under section 903(a)(1) and/or 903(a)(7)(A) of the FD&C Act.
 
The violation discussed in this letter does not necessarily constitute an exhaustive list. You should immediately correct the violation that is referenced above, as well as violations that are the same as or similar to the one stated above, and take any necessary actions to bring your tobacco products into compliance with the FD&C Act. 
 
It is your responsibility to ensure that your 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 ensure full compliance with the FD&C Act may result in FDA initiating further action without notice, including, but not limited to, civil money penalties, criminal prosecution, seizure, and/or injunction. Please note that any adulterated and misbranded tobacco products offered for import into the United States are subject to detention and refusal of admission.
  
Unfair or Deceptive Marketing
 
In addition, the Federal Trade Commission has reviewed the online marketing of Patches by Candy Co. e-liquid. Section 5 of the FTC Act prohibits unfair or deceptive acts or practices in or affecting commerce. This prohibition includes practices that present unwarranted health or safety risks. Commission Policy Statement on Unfairness, 104 F.T.C. 1070, 1071 (1984) (appended to Int’l Harvester Co., 104 F.T.C. 949 (1984)), available at https://www.ftc.gov/public-statements/1980/12/ftc-policy-statement-unfairness. Preventing practices that present unwarranted health and safety risks, particularly to children, is one of the Commission’s highest priorities. FTC Strategic Plan for 2018-2022, at 6; Philip Morris, Inc., 82 F.T.C. 16 (1973).
 
As noted above, Patches by Candy Co. e-liquid is marketed in packaging that closely resembles candy such as Sour Patch Kids, a brand that is very popular with young children. Patches by Candy Co. e-liquid has a scent very similar to Sour Patch Kids candy products and the odor is detectible without opening the packaging. Given the significant number of serious child poisonings due to the ingestion of liquid nicotine, packaging Patches by Candy Co. e-liquid in a manner that is likely to be particularly appealing to young children could present an unwarranted risk to health and safety.
 
The FTC strongly urges you to review your marketing, including packaging, for Patches by Candy Co. e-liquid and similarly marketed products and to take swift and appropriate steps to protect consumers, especially young children.
 
Conclusion and Requested Actions
 
With regard to the FD&C Act violation described in this letter, please submit a written response to this letter within 15 working days from the date of receipt describing your corrective actions, including the dates on which you discontinued the violative labeling, advertising, sale, and/or distribution of these tobacco products and your plan for maintaining compliance with the FD&C Act. If you do not believe that your products are in violation of the FD&C Act, include your
 
reasoning and any supporting information for our consideration. You can find the FD&C Act through links on FDA’s homepage at http://www.fda.gov.
 
Please note your reference number, RW1800852, in your response and direct your response 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, please contact Ele Ibarra-Pratt at (301) 796-9235 or via email at CTPCompliance@fda.hhs.gov.   
 
With regard to the FTC-related issues described above, please notify Rosemary Rosso of the FTC via electronic mail at rrosso@ftc.gov within 15 days of receipt of this letter of the specific actions you have taken to address the FTC’s concerns.
 
 
Sincerely,
 
/S/
Ann Simoneau, J.D.
Director
Office of Compliance and Enforcement
Center for Tobacco Products
 
 
 
/S/ 
Mary K. Engle
Associate Director
Division of Advertising Practices
Federal Trade Commission
 
 
VIA UPS and Electronic Mail
 
cc:
 
Allen Park
ACH Group, LLC d/b/a Candy Co E-Liquids
10941 Hayford St
Norwalk, CA 90650
 
GoDaddy.com, LLC
abuse@godaddy.com

 

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