Supplements

threatened with jail time for “practicing nutrition without a license”

By Jack Minor
A blogger in North Carolina has been threatened with jail time for “practicing nutrition without a license” by writing about his experiences with diabetes and telling readers what types of food he was eating.

It was in January when the North Carolina Board of Dietetics and Nutrition told blogger Steve Cooksey, who writes at diabetes-warrior.net, that it was investigating him for providing nutrition care services without a license.

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Confessions of a Frustrated Pharmacist

by Stuart Lindsey, PharmD.

When an insider breaks ranks with pharmaceutical orthodoxy, it is time to take notice. "Whistleblower" may be an overused term, but the article that follows might be well worth readers' consideration before standing in line for their next prescription refill. - Andrew W. Saul, OMNS Editor

No Deaths from Vitamins: America's Largest Database Confirms Supplement Safety

(OMNS, Dec 28, 2011) There was not even one death caused by a vitamin supplement in 2010, according to the most recent information collected by the U.S. National Poison Data System.

The FDA New Dietary Ingredients Guidance

The Food and Drug Administration (FDA) has recently commenced a new assault against the dietary supplement industry – one that could threaten the availability of supplements currently on the market and that will discourage manufacturers from innovating new and more beneficial products in the future. In July the agency issued a draft Guidance document which sets forth its current thinking concerning provisions of the law that dictate what ingredients can be included in dietary supplement products, and what information companies must submit to the FDA if they desire to market a supplement that contains a new dietary ingredient (i.e., one that was not sold prior to October 15, 1994).

The FDA’s draft Guidance ignores the intent of Congress by seeking to impose insurmountable obstacles to the introduction of new dietary ingredients and includes interpretations that will threaten the continued sale of supplements if even the most minute of changes are made. If the Guideline is finalized and enforced by the FDA it will go a long way towards establishing the agency’s long-standing goal of requiring pre-market approval for dietary supplements.

The following are a few highlights of the Guidance document:

God help the allopathic system

79 Year Old Mother Doing GREAT
After 5 Years on Program

Hi, Felisa -

Thank you for this info - it will be helpful!  I just now faxed Vera's four-page blood test results from May.  Everything is looking great except for the viral load, which isn't sky high - but does demonstrate that she needs to be staying on top of things!  We really appreciate Lloyd looking the results over and giving a recommendation.  Are we at the point where Vera can go on a "maintenance" plan - or do we need to go back at it pretty hard in order to knock the viral count down to near zero?  I would MUCH rather be radical now, when Mom is feeling good, than wait until things flare up. 

FDA's scheme to outlaw all nutritional supplements created after 1994 would destroy millions of jobs and devastate economy

Yesterday we reported on the FDA's new scheme for outlawing nearly all nutritional supplements formulated after October, 1994 (http://www.naturalnews.com/032912_F...). That was just the beginning of this story, because a detailed analysis of the proposed new regulation reveals extremely disturbing revelations that would absolutely gut the nutritional products industry if these regulations are put into practice.

FDA’s New Sneak Attack on Supplements

Just before the July 4 holiday weekend, hoping to limit media attention, the FDA dropped a bomb on dietary supplements. Don’t let them get away with it! A new Action Alert.

On July 1, the US Food and Drug Administration issued draft guidance for complying with the New Dietary Ingredient (NDI) notification protocols contained in the Dietary Supplement Health and Education Act (DSHEA). Ever since DSHEA was enacted in 1994, supplement manufacturers have had very little guidance on what counts as an NDI and when or how to send an NDI notification. The government has arbitrarily ignored or enforced this section of DSHEA, doing as it liked, without spelling out the rules.

Why does this matter? Because when you hear New Dietary Ingredient (NDI), substitute “New Supplement” in your mind. What we are dealing with here is whether the supplement industry is allowed to innovate and create new supplements—and if so, under what rules.

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