Company: Daniel Chapter One Inc
Subject: New Drug/Labeling/False & Misleading Claims
Issuer: New England District Office
Issued: Aug. 15, 2008 Closed:
Not applicable.
Source ucm1048176 Archive Code:

Daniel Chapter One Inc 15-Aug-08

Department of Health and Human Services

Public Health Service
Food and Drug Administration

New England District
One Montvale Avenue
Stoneham, Massachusetts 02180
(781) 596-7700
FAX: (781) 596-7896




August 15, 2008

Mr. James J Feijo
Daniel Chapter One Inc
2749 East Main Road
Portsmouth, RI 02871

1028 East Main Road
Portsmouth, RI 02871

P.O. Box 223
Portsmouth, RI 02871

Dear Mr. Feijo:

This is to advise you that the Food and Drug Administration (FDA) has reviewed your websites at the Internet addresses,, and and has determined that the products "7 Herb TM Formula," "Apple Pectin Plus," and "CoQ10" are promoted for conditions that cause the products to be drugs under section 201 (g)(1)(B) of the Federal Food, Drug, and Cosmetic Act (the Act) [21 U.S.C. § 321 (g)(1)(13)). The therapeutic claims on your websites establish that the products are drugs because they are intended for use in the cure, mitigation, treatment, or prevention of disease. The marketing of these products with these claims violates the Act.

Examples of some of the claims observed on your web sites include:

7 Herb™ Formula

In description of ingredients:

• "Burdock Root, used in Ayurvedic and Chinese medicine to treat cancer. It is known to decrease cell mutation and inhibit tumors."
• "Sheep Sorrel is a traditional folk remedy for cancer."
• "Cat's Claw is used by native Peruvians to treat many diseases, including cancer."
• "Studies done in the 1980s show Turkey Rhubarb has anti-tumor properties."

Examples of claims in the form of testimonials include:

• "I had a mass in my left breast . . . I was already taking GDU & Bio C-500 so, as per Jim & Trish's advice I added 7 Herb Formula and Bio Shark. After I began taking these products it (the lump) began to shrink . . . . In January 20081 had a mammogram done which showed it (the lump) was cancer. After talking with Jim and Trish again about this they increased the amount of GDU, Bio Chark [sic], & 7 Herb Formula tremendously. It really shrunk alot then and kept on shrinking."
• "My son was diagnosed with a tumor on his left temple. The tumor was extremely aggressive . . . . [A] friend suggested we speak to Jim and Tris. They suggested 7 HerbTM Formula, BioShark and GDUTM Caps, which we bought and started him on. . . .[I]n the time it took us to find a specialist who eventually told us he could not help either, the tumor had already begun to shrink . . . . Four months later the whole family is using the products, as well as my patients, and you would never know my son had a tumor."
• "I had contracted leukemia and had three inoperable tumors. When I decided not to do chemotherapy or radiation, my father sent me Bio*Mixx and 7 Herb Formula . . . I am now in complete remission. The cancer cell count has dropped, the doctors tell me."

Apple Pectin Plus

• "Apple Pectin Plus can help reduce the risk of colon, breast and prostate cancer."


• "CoQ10 deficiency has been linked to such diverse conditions as heart disease, heart failure, hypertension, muscular dystrophy, cancer . . . diabetes, obesity, periodontal disease . . . ."

Your products are not generally recognized as safe and effective for the above referenced uses and, therefore, the products are "new drugs" under section 201(p) of the Act [21 U.S.C. § 321(p)]. New drugs may not be legally marketed in the U.S. without prior approval from FDA as described in section 505(a) of the Act [21 U.S.C. § 355(a)]. FDA approves a new drug on the basis of scientific data submitted by a drug sponsor to demonstrate that the drug is safe and effective. Your products "7 HerbTM Formula," "Apple Pectin Plus," and "CoQ10" are also misbranded within the meaning of section 502(f)(1) of the Act in that labeling for these drugs fails to bear adequate directions for use [21 U.S.C. § 352(f)(1)).

The above violations are not meant to be an all-inclusive list of deficiencies in your products and their labeling. While reviewing your websites, we noticed that you were promoting the products listed above for the treatment and/or prevention of diseases other than cancer. Additionally, while reviewing these websites and other websites that you operate, including,,, and, we noticed that you were promoting other products for disease treatment and/or prevention. The, unlawful disease treatment and prevention claims on your websites were too numerous to list in this letter. It is your responsibility to ensure that products marketed by your firm comply with the Act and its implementing regulations. We advise you to review your websites, product labels, and other labeling and promotional materials for your products to ensure that the claims you make for your products do not cause them to violate the Act.

You should take prompt action to correct the violations described above and prevent their future recurrence. Failure to do so may result in enforcement action without further notice. The Act authorizes the seizure of illegal products and injunctions against manufacturers and distributors of those products [21 §§ U.S.C. 332 and 334].

Please notify this office, in writing, within fifteen (15) working days of the receipt of this letter, as to the specific steps you have taken to correct the violations noted above and to assure that similar violations do not occur. Include any documentation necessary to show that correction has been achieved. 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 response should be directed to Bruce R. Ota, Compliance Officer at the above address.



John R. Marzilli
Acting District Director
New England District