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What to Say to the FDA
Written By: Jim and Resa Johnson - Cashiers Chiropractic and Acupuncture | Issue: 2016/12 - December
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Are you like me, do you do as much as you possibly can to do make the right health choices?
Are you someone who takes a natural approach, which might mean that you take supplements, herbs, and other remedies instead of drugs that are toxic with a few beneficial side effects? The Food and Drug Administration would like you to take more of the drug route!
On August 11, the FDA issued its revised New Dietary Ingredient Draft Guidelines. These new guidelines require, among many other things, that all dietary ingredients introduced into the marketplace since October 15, 1994, undergo drug-like safety testing prior to marketing. The tests, which are actually more onerous than those for new drugs, could cost millions of dollars per each new ingredient. If you Google “Death from Vitamins,” you’ll find that over the past 27 years — the complete time frame that the data has been available — there have been zero deaths as a result of vitamins and over three million deaths related to prescription drug use.
Let’s be honest with ourselves — the real reason for the FDA’s Draft Guidelines has nothing to do with safety, but rather to drive more supplements off the shelves, increase the costs to consumers, and bankrupt the small dietary supplement companies, thus paving the way for the large pharmaceutical industry to use the same ingredients with now skewed molecular structures, to sell them as drugs at premium prices.
Keep pressure on the FDA, write Congress at act.thenhf.com. Contact the National Health Federation at [email protected]. I want to thank Scott C Tips, legal counsel for the National Health Federation and this article in The Townsend Letter for bringing this to our attention.
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