Inspections, Compliance, Enforcement, and Criminal Investigations
Algisiya Servicesz Limited
Department of Health and Human Services
|Public Health Service
Food and Drug Administration
|Center for Tobacco Products
9200 Corporate Boulevard
Rockville MD 20850-3229
FROM: Food and Drug Administration
RE: Camel Orange/Mild Cigarettes
DATE: November 2, 2009
This is to advise you that the United States Food and Drug Administration (FDA) reviewed your website at the Internet address www.dutyfreedepot.com on September 29, 2009, and determined that your website has been offering for sale Camel Orange/Mild Cigarettes to consumers in the United States. Under section 201 (rr) of the Federal Food, Drug, and Cosmetic Act (FFDCA), as amended by the Family Smoking Prevention and Tobacco Control Act (FSPTCA), 21 U.S.C. § 321(rr), these products are tobacco products because they are made or derived from tobacco and intended for human consumption.
According to the information and materials on your website we reviewed, your product listed above contains an artificial or natural flavor that is a characterizing flavor of the product and, as such, is adulterated and/or misbranded. Section 907(a)(1)(A) of the FFDCA, 21 U.S.C. § 387g(a)(1)(A), provides, as part of the tobacco product standards, a "special rule for cigarettes" as follows:
[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, including strawberry, grape, orange, clove, cinnamon, pineapple, vanilla, coconut, licorice, cocoa, chocolate, cherry, or coffee, that is a characterizing flavor of the tobacco product or tobacco smoke.
After the September 22,2009 effective date for this provision, flavored cigarettes marketed and sold in the United States in violation of this provision are adulterated under section 902(5) of the FFDCA, 21 U.S.C. § 387b(5).
Your website represents that Camel Orange/Mild Cigarettes contains orange/mild flavor that is a characterizing flavor of the tobacco product. A review of your website revealed information about this product as follows:
• Described as "Camel Orange/Mild Cigarettes;"
• Labeled "Camel ORANGE" with a color photograph of product packaged with orange colored labeling; and
• Offered for sale to U.S. consumers
If Camel Orange/Mild Cigarettes contains orange/mild flavor that is a characterizing flavor of the tobacco product, your Camel Orange/Mild Cigarettes is adulterated under section 902(5) of the FFDCA, 21 U.S.C. § 387b(5), because it fails to comply with the special rule for cigarettes detailed in section 907(a)(1)(A) of the FFDCA, 21 U.S.C. § 387g(a)(1)(A). If, however, Camel Orange/Mild Cigarettes does not contain a flavor, herb, or spice that is a characterizing flavor of the tobacco product, it is misbranded under section 903(a)(1) of the FFDCA, 21 U.S.C. § 387c(a)(1), as its labeling is false and misleading because it makes the representation that the product contains orange/mild flavor that is a characterizing flavor of the tobacco product.
You should immediately correct this violation by ceasing the marketing and sale of your product or taking other appropriate action to bring your product into compliance with the requirements of the FFDCA. Failure to correct this violation may result in regulatory action being initiated by the FDA without further notice. These actions may include, but are not limited to, seizure and injunction.
If you are not located in the United States, please note that adulterated or misbranded tobacco products offered for importation into the United States are subject to detention and refusal of admission. We will advise the appropriate regulatory or law enforcement officials in the country from which you operate that FDA considers your product listed above to be an adulterated and/or misbranded product that cannot be legally sold to consumers in the United States.
Please submit a written response to this letter within 15 working days from the date you receive this letter, describing your intent to comply with this request and explaining your plan for discontinuing the marketing and sale, or relabeling, of this tobacco product. Please direct your response to Ann Simoneau, Regulatory Counsel, Center for Tobacco Products, Food and Drug Administration, 9200 Corporate Boulevard, Rockville, 'Maryland 20850, (240) 276-4017, or send via email to FDAFlavoredCigaretteTaskForce@FDA.HHS.GOV. We remind you that only written communications are considered official.
The violation discussed in this letter does not necessarily constitute an exhaustive list. It is your responsibility to ensure that your tobacco products comply with the applicable provisions of the FFDCA, as amended by the FSPTCA, that are currently in effect.
Lawrence R. Deyton, M.S.P.H., M.D.
Director, Center for Tobacco Products