Mike Adams & Alex Jones: The FDA’s End Game!!

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• FDA’s scheme to outlaw nearly all nutritional supplements created after 1994 would destroy millions of jobs and devastate economy!
  (NaturalNews) 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.
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  Below are the highlights of the most offensive and onerous portions of these proposed new FDA regulations. The source of all this information is the FDA itself, which proposes its new rules in a rather lengthy post at: http://www.fda.gov/Food/GuidanceCom…
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  • Every nutritional supplement company will be forced to submit omprehensive NDI (New Dietary Ingredient) documentation for EACH ingredient used in EACH product they currently sell. This will amount to hundreds of thousands of NDI applications flooding the FDA offices. This is a clever FDA scheme to place a huge burden of research and paperwork on every dietary supplement company in the USA. In the FDA’s own words:
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  “The statute places the obligation for submitting the notification on each manufacturer or distributor. Any other manufacturer or distributor who wishes to market its own dietary supplement containing the same NDI should submit a NDI notification to FDA explaining its own basis for concluding that this new product containing the NDI will “reasonably expected to be safe” under the conditions recommended or suggested in the new product’s labeling.”
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  • All supplement companies must REMOVE their products from “interstate commerce” for the 75 days after the FDA receives their NDI applications. No product containing an NDI application ingredient may be sold in the United States or it will be considered “adulterated” by the FDA and thereby subjected to confiscation.
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  • While the NDI provisions of the 1994 DSHEA act merely required dietary supplement companies to notify the FDA of new ingredients, the FDA is now distorting this into a de facto supplement approval process. Without the FDA’s new approval, nutritional supplements will all be labeled “adulterated” and potentially confiscated at gunpoint by the FDA (see FDA raid links below).
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  • The FDA does not support electronic filing for NDI applications. All applications must be done on paper and then mailed to the FDA (yes, as in dropped in a metal mailbox with a paper envelope). The 75 days of waiting does not begin until the FDA says it receives your application.
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  …. for the full article click here!

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