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To tell the truth.


Challenging FDA FDA
abbr.
Food and Drug Administration


FDA,
n.pr See Food and Drug Administration.

FDA,
n.pr the abbreviation for the Food and Drug Administration.
 censorship

If you sell nutritional supplements Nutritional Supplements Definition

Nutritional supplements include vitamins, minerals, herbs, meal supplements, sports nutrition products, natural food supplements, and other related products used to boost the nutritional content of the diet.
 in the United States and you want to tell consumers about the benefits of your product, you have to get permission from the Food and Drug Administration. There are thousands of true statements you could make about the health effects of nutrients, but the FDA has approved only two: that calcium helps prevent osteoporosis, and that folic acid folic acid: see coenzyme; vitamin.
folic acid
 or folate

Organic compound essential to animal growth and health and needed by bacteria as a growth factor.
 reduces the risk of neural-tube birth defects birth defects, abnormalities in physical or mental structure or function that are present at birth. They range from minor to seriously deforming or life-threatening. A major defect of some type occurs in approximately 3% of all births. . Both claims were approved years after they were widely accepted by the scientific community.

In the nine years it took the FDA to approve the calcium claim and the three years it took to approve the folic acid claim, thousands of people suffered from osteoporosis and thousands of babies were born with neural-tube defects. Durk Pearson and Sandy Shaw, who design dietary supplements and license manufacturers to produce them, note that many of these cases might have been prevented by information the FDA blocked. Alarmed by the harmful and potentially deadly consequences of the FDA's labeling restrictions, Pearson and Shaw are challenging the agency's censorship in federal court.

Pearson and Shaw want to label their products with truthful statements based upon substantial scientific evidence, such as:

* "Consumption of antioxidant vitamins in the amounts contained in this product may reduce the risk of certain kinds of cancers."

* "Consumption of 25 to 35 grams per day of dietary fiber dietary fiber
n.
Coarse, indigestible plant matter, consisting primarily of polysaccharides, that when eaten stimulates intestinal peristalsis.
 may reduce the risk of colorectal cancer colorectal cancer

Malignant tumour of the large intestine (colon) or rectum. Risk factors include age (after age 50), family history of colorectal cancer, chronic inflammatory bowel diseases, benign polyps, physical inactivity, and a diet high in fat.
."

* "Consumption of omega-3 fatty acids This is a list of omega-3 fatty acids.

Common name Lipid name Chemical name
α-Linolenic acid (ALA) 18:3 (n-3) octadeca-9,12,15-trienoic acid
Stearidonic acid 18:4 (n-3) octadeca-6,9,12,15-tetraenoic acid
 may reduce the risk of coronary heart disease coronary heart disease: see coronary artery disease.
coronary heart disease
 or ischemic heart disease

Progressive reduction of blood supply to the heart muscle due to narrowing or blocking of a coronary artery (see atherosclerosis).
."

Despite the cautious phrasing, the FDA considers such statements misleading, since the evidence supporting these associations is not conclusive (as Pearson and Shaw concede). The agency requires "significant scientific agreement" before approving a health claim, a standard it defines "on a case-by-case basis."

Represented by Washington, D.C., attorney Jonathan Emord, Pearson and Shaw argue that the FDA's rules amount to prior restraint and violate the commercial speech doctrine. They add that the restrictions are in any case too broad, since they apply not only to labeling in the narrow sense but also to books, scientific articles, or summaries of research displayed or distributed near dietary supplements (in a health food store, for example). They charge that the lack of a clear standard for approving health claims violates both the Fifth Amendment's Due Process Clause and the Nutrition Labeling and Education Act of 1990.

Pearson and Shaw first filed their suit in the U.S. Court of Appeals for the Ninth Circuit, which decided it did not have jurisdiction. Commenting that the "petition is far from frivolous," it referred the case to the U.S. District Court in Washington, D.C., which is scheduled to hear oral arguments on April 30.
COPYRIGHT 1996 Reason Foundation
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 1996, Gale Group. All rights reserved. Gale Group is a Thomson Corporation Company.

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Title Annotation:Food and Drug Administration's labeling laws
Author:Sullum, Jacob
Publication:Reason
Date:Apr 1, 1996
Words:451
Previous Article:Statist quo. (regulatory reform)
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