Department of Health and Human Services' logo Department of Health and Human Services

Public Health Service
Food and Drug Administration
Denver District Office

 

Bldg 20, Denver Federal Ctr
6th Ave & Kipling St
Denver, CO 80225-0087
Telephone: 303-236-3000
Fax: 303-236-3551

July 19, 2006
WARNING LETTER
VIA CERTIFIED MAIL, RETURN RECEIPT REQUESTED

Larry Graziani
Betterthanair
PO Box 2488
35715 US Hwy 40 #D103
Evergreen, CO 80437

Ref. No. DEN-06-21

Dear Mr Graziani:

This letter concerns your firm's marketing of the "BetterThanAir™ oxygen enriched products" on your website, www.betteranair.com. According to information on your website, the "BetterThanAir™ oxygen enriched products" referred to as: "Oxygen Kit," "O_PurlBO-8L," "B1ueAir," "P024U Personal Oxygen System," "P024U Refill," "'O' 2 Go!," "BlueAir 2L," "Oxycan," "Oxygen Shot," "3rd Lung Kit," "BetterThanAir Emergency Oxygen M6 Travel Unit," "BetterThanAir Emergency Oxygen M9 Travel Unit," "Hangover Air," and "O_Pur/Eucalyptus," are intended to prevent, treat, or cure disease conditions or to affect the structure or any function of the body. The statements on your website that document these intended uses include, but are not limited to, the following:

"BetterThanAir™ oxygen enriched products" are drugs, as defined by Section 201(g)(1) of the Federal Food, Drug, and Cosmetic Act (Act), [21 USC 321(g)(1)], because they are intended for use in the diagnosis, cure, mitigation, treatment, or prevention of disease and to affect the structure or function of the body.

Moreover, these products are new drugs, as defined by section 201(p) of the Act, [21 USC 321(p)], because they are not generally recognized as safe and effective for their labeled uses. Under sections 301(d) and 505(a) of the Act, [21 USC 331(d) and 355(a)], a new drug may not be introduced or delivered for introduction into interstate commerce unless an FDA-approved application is in effect for it. Your sale of "BetterThanAir™ oxygen enriched products" without such approved applications violates these provisions of the Act.

Further, these oxygen products are also prescription drugs within the meaning of section 503(b)(1) of the Act, [21 USC 353(b)(1)], because they are not safe for use except under the supervision of a practitioner licensed by law to administer such drugs. The "BetterThanAir™ oxygen enriched products" are misbranded within the meaning of section 503(b)(1) and 503(b)(4) of the Act, [21 USC 353(b)(1) and 353(b)(4)] because they are marketed without a prescription and they lack the statement, "Rx only." The inclusion of the disclaimer, "Not for medical and prescription use," on the product's label does not remove the product from the prescription dispensing requirement of section 503(b)(2) of the Act [21 USC 353(b)(2)].

Furthermore, because these products are offered for use for conditions that are not amenable to self-diagnosis and treatment by individuals who are not medical practitioners, adequate directions cannot be written so that a layperson can use these products safely for their intended uses. Thus, the "BetterThanAir™ oxygen enriched products" labeling fails to bear adequate directions for their intended uses, causing them to be misbranded under Section 502(f)(1) of the Act, [21 USC 352(f)(1)]. These products are not exempt from the adequate directions for use requirement because they do not meet the conditions set forth in 21 CFR 201.100.

Furthermore, these products are misbranded under section 502(o) of the Act, [21 USC 352(o)] because the "BetterThanAir™ oxygen enriched products," are not listed as required by Section 510(i)(1) and (j)(1) of the Act [21 USC 360(i)(1) and (j)(1)].

"BetterThanAir™ oxygen enriched products" are also subject to the Current Good Manufacturing Practice (CGMP) regulations at 21 CFR Parts 210 and 211. They may be considered adulterated under section 501(a)(2)(B) of the Act, [21 USC 351(a)(2)(B)], if the methods used in, or the facilities or controls used during the product's manufacture, processing, packing, or holding do not conform to, or are not operated or administered in conformity with CGMP.

The above violations are not intended to be an all-inclusive list of deficiencies. It is your responsibility to ensure that the drug products that you manufacture, or distribute, meet all of the requirements of the Act and its implementing regulations. Federal agencies are advised of the issuance of all warning letters about drugs and devices so that they may take this information into account when considering the award of contracts.

You must immediately correct these violations. If you do not immediately correct them, you may be subject to FDA enforcement action without further notice. The Act provides for seizure of illegal products and for an injunctive relief against the manufacturers and distributors of illegal products. You must notify FDA in writing within 15 working days of receipt of this letter as to the steps that you have taken to correct the above-listed violations of the Act and its implementing regulations, and the steps taken to assure that similar violations will not recur. If corrective action cannot be completed within 15 working days, state the reason for the delay and the time within which the corrections will be made. Further, if your firm does not manufacture the products identified above, your reply should include the name and address of the manufacturer. If the firm from which you receive the product is not the manufacturer, please include the name of your supplier in addition to the manufacturing firm.

Your response should be directed to: Food and Drug Administration, Denver District, PO Box 25087, Denver, CO 80225-0087, Attn: William H. Sherer, Compliance Officer. If you have any questions, please contact Mr Sherer at (303) 236-3051.

Sincerely,
/s/
B. Belinda Collins
District Director

This page was posted on February 12, 2008.

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