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U.S. Department of Health and Human Services

Inspections, Compliance, Enforcement, and Criminal Investigations

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Chozyn, LLC 29-Nov-05

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

Public Health Service
Food and Drug Administration

 

Central Region
New Jersey District
Waterview Coporate Center
10 Waterview Blvd., 3rd Floor
Parsippany, NJ 07054



Warning Letter

CERTIFIED MAIL
RETURNED RECEIPT

November 29, 2005

File #: 06-NWJ-07

Jeffrey Jordan
Chozyo, LLC
984 Route 9 South, Suite 11
Parlin, NJ 08859

Dear Mr: Jordan:

The Food and Drug Administration (FDA) has reviewed your website at the Internet address http://www.neugenisis.com and has concluded that claims in the labeling for your product Lingoji cause the product to be a drug as defined in section 201(g)(1)(B) of the Federal Food, Drug, and Cosmetic Act (the Act) [21 U.S.C. 321 (g)(1)(B)]. You can find the Act and FDA's regulations through links on FDA's Internet homepage: http://www.fda.gov.

Under the Act, articles intended for use in the diagnosis, cure, mitigation, treatment or prevention of disease in man are drugs [Section 201 (g)(1)(B) of the Act, 21 U.S.C. 321 (g)(1)(B)]. Your website claims that your product is useful in the prevention and treatment of avian flu and other forms of influenza.

The Internet labeling of your product bears the foIIowing claims:

  • " (Under page heading "Lingoji™; from Neulife Laboratories") "As seen on CNN, . PrimeTime, etc. Protect yourself from the Avian Flu. The Nation may be unprepared, according to certain experts, but you can improve your defenses."

  • " (Testimonial) "I have bad a history of bad flu seasons's [sic]. . . the past couple of years. I started taking Liugoji....For the first time in 5 years, I have enjoyed a full season without sickness ."

  • " (Testimonial) "The talk and treat of these epidemis, flu's [sic], etc lead me to my Doctor. He actually recommended Lingoji...I am looking to the flu season WITHOUT the flu."

These claims cause your product to be a drug, as defined in section 201(g)(1)(B) of the Act [21 U.S.C. 321 (g)(1)(B)]. Because your product is not generally recognized as safe and effective when used as labeled, it is also a new drug as defined in section 201(p) of the Act [21 U.S.C. 321(p)]. Under section 505 of the Act [21 U.S.C. 355 (a)], a new drug may not be legally marketed in the United States without an approved New Drug Application (NDA). This drug is also misbranded within the meaning of section 502(a) of the Act [21 U.S.C. 352(a)] because their labeling is false and misleading in that it suggests that this drug is effective for the prevention and treatment of avian flu and other forms of influenza when, in fact, these claims are not supported by competent and reliable scientific evidence.

This letter an all-inclusive review of your website and the products that your form markets. It is your responsibility to ensure that all products marketed by your firm comply with the Act and its implementing regulations.

You must immediately correct these violations. If you do not immediately correct them, you may be subject to enforcement action without notice. The Act provides for seizure of illegal products and for injunctions against the manufacturers and distributors of illegal products [21 U.S.C. 332 and 334]. Individuals and businesses that violate the Act may also be subject to criminal prosecution.

Please advise this office, in writing and within fifteen (15) working days of the receipt of this letter, as to the specific steps you haven taken to correct the violations noted above and to ensure that similar violations do not occur. If corrective actions cannot be completed within fifteen working days, state the reason for the delay and the time within which the corrections will be completed.

Your reply should be addressed to Compliance Officer Andrew Ciaocia at the above address.

Sincerely,

/s/
Douglas I. Ellsworth
District Director