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  5. Liqin Lin - 09/04/2015
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WARNING LETTER

Liqin Lin


Recipient:
Liqin Lin


United States

Issuing Office:
Center for Tobacco Products

United States


  

Department of Health and Human Services logoDepartment of Health and Human Services

Food and Drug Administration
 
Center for Tobacco Products
10903 New Hampshire Avenue
Silver Spring, MD 20993 

 

SEPT 4, 2015

VIA Electronic Mail
 
Liqin Lin
sale@cheapcigarette.cc
 
 
WARNING LETTER
 
Dear Ms. Lin:
 
The Center for Tobacco Products of the U.S. Food and Drug Administration (FDA) recently reviewed the websites http://www.cheapcigarette.cc, http://www.onlinecigarettes.cc, http://www.cigarettes.hk, and http://www.cigarettestore.cc and determined that the cigarette and cigarette tobacco and/or roll-your-own tobacco 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)), as amended by the Family Smoking Prevention and Tobacco Control Act (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 cigarettes, cigarette tobacco, and roll-your-own tobacco, are subject to FDA jurisdiction under section 901(b) of the FD&C Act (21 U.S.C. § 387a(b)).
 
FDA has determined that the websites, http://www.cheapcigarette.cc, http://www.onlinecigarettes.cc, http://www.cigarettes.hk, and http://www.cigarettestore.cc, offer for sale or distribute cigarette tobacco and/or roll-your-own tobacco products. Section 900(4) of the FD&C Act (21 U.S.C. § 387(4)) defines “cigarette tobacco” as “any product that consists of loose tobacco that is intended for use by consumers in a cigarette.” Section 900(15) of the FD&C Act (21 U.S.C. § 387(15)) defines “roll-your-own tobacco” as “any tobacco product which, because of its appearance, type, packaging, or labeling, is suitable for use and likely to be offered to, or purchased by, consumers as tobacco for making cigarettes.”
 
We note that on the websites, http://www.cheapcigarette.cc, http://www.onlinecigarettes.cc, http://www.cigarettes.hk, and http://www.cigarettestore.cc, you present loose tobacco products under the heading “tobacco” that are offered for sale or distributed as cigarette tobacco and/or roll-your-own tobacco, including Port Royal and Rolon. The overall presentation of these products on the websites strongly suggests that they are intended for use in a cigarette, likely to be offered to consumers for making cigarettes, and/or likely to be purchased by consumers for making cigarettes. Specifically, Port Royal Original 5x50g Pack Tobacco has “Premium Rolling Tobacco,” and Rolon Hand Rolling (40g x 10 bags) Tobacco has “HANDROLLING TOBACCO” displayed on their respective packaging. Therefore, the products meet the definition of “cigarette tobacco” and/or “roll-your-own tobacco” in the FD&C Act.

FDA has determined that Kent Deluxe 100’s and Kent HD cigarettes are adulterated under section 902(8) of the FD&C Act (21 U.S.C. § 387b(8)) because they are modified risk tobacco products sold or distributed without an FDA order in effect that permits such sale or distribution. Additionally, FDA has determined that Port Royal Original 5x50g Pack Tobacco and Rolon Hand Rolling (40g x 10 bags) Tobacco cigarette tobacco and/or roll-your-own tobacco products, are adulterated under section 902(5) of the FD&C Act (21 U.S.C. § 387b(5)) or misbranded under section 903(a)(1) of the FD&C Act (21 U.S.C. § 387c(a)(1)) or section 903(a)(7)(A) of the FD&C Act (21 U.S.C. § 387c(a)(7)(A)) because they purport to contain a natural or artificial characterizing flavor.
 
Modified Risk Tobacco Product Violations
 
Our review of the websites, http://www.cheapcigarette.cc, http://www.onlinecigarettes.cc, http://www.cigarettes.hk, and http://www.cigarettestore.cc, revealed that you sell or distribute cigarette products listed or described as being “Lights”or using similar descriptors.  For example, the following cigarette products are listed under the heading “Lights Cigarettes”: Kent Deluxe 100’s and Kent HD.
 
A tobacco product with a label, labeling, or advertising that uses the descriptor “light,” “mild,” “low,” or a similar descriptor, is a “modified risk tobacco product” under section 911(b)(2)(A)(ii) of the FD&C Act (21 U.S.C. § 387k(b)(2)(A)(ii)). Under section 911(a) of the FD&C Act (21 U.S.C. § 387k(a)), no person may introduce or deliver for introduction into interstate commerce any modified risk tobacco product without an FDA order in effect under section 911(g) of the FD&C Act (21 U.S.C. § 387k(g)). A product that is in violation of section 911(a) of the FD&C Act (21 U.S.C. § 387k(a)) is adulterated under section 902(8) of the FD&C Act (21 U.S.C. § 387b(8)). 
 
The above listed products are modified risk tobacco products because the websites use the descriptor “Lights” or similar descriptors to describe these products. Because these products are sold or distributed to customers in the United States without an appropriate FDA order in effect under section 911(g) of the FD&C Act (21 U.S.C. § 387k(g)), these products are adulterated under section 902(8) of the FD&C Act (21 U.S.C. § 387b(8)).
 
Flavored Cigarette Violations
 
Additionally,our review of the websites, http://www.cheapcigarette.cc, http://www.onlinecigarettes.cc, http://www.cigarettes.hk, and http://www.cigarettestore.cc, revealed that you offer for sale or distribute the following cigarette tobacco and/or roll-your-own tobacco products: Port Royal Original 5x50g Pack Tobacco (rum & wine) and Rolon Hand Rolling (40g x 10 bags) Tobacco (mango).
 
These products are purported to contain an artificial or natural flavor that is a characterizing flavor of the products. Section 907(a)(1)(A) of the FD&C Act (21 U.S.C. § 387g(a)(1)(A)) provides:
 
[A] cigarette or any of its component parts (including the tobacco, filter, or paper) shall not contain, as a constituent (including a smoke constituent) or additive, an artificial or natural flavor (other than tobacco or menthol) or an herb or spice . . . that is a characterizing flavor of the tobacco product or tobacco smoke.
 
Cigarettes and cigarette tobacco and/or roll-your-own tobacco that are distributed or sold in the United States in violation of this provision are adulterated under section 902(5) of the FD&C Act (21 U.S.C. § 387b(5)).  Thus, your flavored cigarette tobacco and/or roll-your-own tobacco products areadulterated under section 902(5) of the FD&C Act (21 U.S.C. § 387b(5)).
 
If, however, these cigarette tobacco and/or roll-your-own tobacco products do not contain a characterizing flavor, they are misbranded under section 903(a)(1) of the FD&C Act (21 U.S.C. § 387c(a)(1)) or section 903(a)(7)(A) of the FD&C Act (21 U.S.C. § 387c(a)(7)(A)) as their labeling or advertising is false or misleading because it makes the representation that the products contain, for example, rum & wine or mango as a characterizing flavor of the tobacco products.
 
Conclusion and Requested Actions
 
The violations discussed in this letter do not necessarily constitute an exhaustive list. You should immediately correct the violations that are referenced above, as well as violations that are the same as or similar to those 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 these websites, on any other websites (including e-commerce, social networking, or search engine websites), and in any other media in which you advertise 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, no-tobacco-sale orders, criminal prosecution, seizure, and/or injunction. Please note that adulterated and misbranded tobacco products offered for import into the United States are subject to detention and refusal of admission.
 
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. You can find the FD&C Act through links on FDA’s homepage at http://www.fda.gov.
 
Please note your reference number, RW1500356, 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 about the content of this letter, please contact Ele Ibarra-Pratt at (301) 796-9235 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 Electronic Mail
 
cc:
 
http://www.cheapcigarette.cc, http://www.onlinecigarettes.cc, http://www.cigarettes.hk
cheapcigarette8899@hotmail.com
 
http://www.cigarettes.hk
cigarettes.hk@hotmail.com
 
http://www.cigarettestore.cc
cigarettestore.cc@hotmail.com
 
Sophie Lin
nikesellorder@hotmail.com
 
Jinsheng Weng
yangpangpang99@163.com
 
Fujianzhong
505174048@qq.com
 
Hichina Zhicheng Technology Ltd.
admin@hichina.com
abuse@list.alibaba-inc.com
 
Hong Kong Domain Name Registration Company
enquiry@hkdnr.hk
 
Simple Helix
admin@simplehelix.com
support@simplehelix.com