Natural News
By Mike Adams, The Health Ranger
Thursday July 7th 2011

(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.
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...
•  Every nutritional supplement company will be forced to submit  comprehensive 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:
"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."
•  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.
• 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).
• 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.
•  While a few ingredients that were in widespread use before 1994 are  exempted from these new requirements, the FDA refuses to publish any  list of "grandfathered" ingredients. Instead, it requires each  supplement company to figure it out for themselves. In addition, even  pre-1994 ingredients must receive 
new approvals from the FDA if  they are "altered" in any way, including changing the particle size,  increasing the amount per serving, using a super-critical extraction  process, baking the substance or even harvesting it from a plant at a  different life stage of the plant. In other words, nearly all  ingredients use in dietary supplements today are considered  "adulterated" by the FDA.
• As a result of the point above,  nearly all dietary ingredients will be required to receive new approval  by the FDA due to the agency's broad definition of "adulterated." Note  that 
changing the mg per serving of the nutrient makes it  "adulterated," as does altering the target market. So if you sell  vitamin C to senior citizens, and it's approved by the FDA as a dietary  ingredient, you will need a NEW application and approval if you now sell  that same vitamin C to children.
• The requirements for  "proving" the safety and efficacy of dietary ingredients is entirely  unreasonable. FDA says it requires companies to submit peer-reviewed  scientific journal articles, clinical trial test results and even, in  the case of botanicals, to provide the name of the scientist who  originally gave the plant its Latin name. (Seriously? Is it a trick  question?)
• The FDA has 
no obligation to "approve" any NDIs in a timely manner. It merely says it will acknowledge receipt of the NDI application within 
75 days.
•  If one company receives approval for a specific dietary ingredient  (resveratrol, for example), that approval does NOT apply to any other  company. 
EVERY company must independently apply for approval of  resveratrol, and each company must independently supply all the research  and documentation required to support the safety and efficacy of that  ingredient 
in the amounts used in its products, and 
in the context of the marketing of that product.
•  Companies that sell dietary supplements containing ingredients that  have not been approved under these new FDA regulations will be accused  of selling "adulterated" ingredients and can have their inventory seized  by federal marshals or have their company founders arrested for selling  "adulterated drugs" even though they might only be vitamins or herbs.
•  These proposed regulations are NOT a law under the control of Congress.  Neither the House nor the Senate has any control over this. The FDA can  simply issue these regulations on its own, regardless of what publicly  elected officials want the agency to do. The FDA is run by 
unelected bureaucrats who answer to no one and write their own "laws." (See attorney Jonathan Emord's book 
The Rise of Tyranny to learn more.)
•  The FDA can simply choose to DENY all applications and thereby outlaw  virtually all nutritional supplements. There is no obligation by the FDA  to honestly and accurately review any applications whatsoever. It can  simply rubber stamp 'DENIED' on every one of them. In the FDA's own  words: "FDA's failure to respond to a NDI notification does not  constitute a finding by the agency that the NDI or the dietary  supplement containing the NDI is safe or is not adulterated."
• The real kicker in all this? 
Synthetic molecules  that mimic dietary supplements (i.e. those used in pharmaceuticals) are  EXEMPTED from all these requirements! So synthetic molecules need no  approval from the FDA, while the natural ones do! This conveniently  exempts the 
pharmaceutical vitamin companies who use synthetic vitamin chemicals rather than natural, full-spectrum nutrients.
The FDA's plan to kill the supplement industry with a thousand paper cuts
This is all revealed on the FDA's own proposed regulation page:
http://www.fda.gov/Food/GuidanceCom...
A sample form for requesting NDI "approval" is available at:
http://www.fda.gov/downloads/Food/G...
Remember, the FDA will receive 
hundreds of thousands of these applications  if it adopts this regulation. Under that mountain of paperwork, guess  what we'll see next? The FDA begging Congress for "more money" to handle  the work load!
The FDA also provides a 
decision chart to help you decide whether your ingredient needs to seek FDA approval:
http://www.fda.gov/downloads/Food/G...
Notice  that nearly ALL ingredients lead to the conclusion of "NDI notification  required." And even for those ingredients that the FDA says don't  require notification, it recommends voluntary notification (bottom right  corner of the chart).
Note carefully, too, that merely altering the 
intake level  of a nutrient is enough to require new FDA notification and approval!  So merely increasing the level of omega-3s in a supplement will require a  manufacturer to seek a new approval from the FDA.
The FDA will turn vitamin company founders into wanted criminals
Also note: 
All products made with ingredients that are not APPROVED by the FDA under these new rules will be called ADULTERATED. The FDA has a long history of engaging in 
armed raids against companies that it accuses of selling "adulterated" products (
http://www.naturalnews.com/021791.html).
Owners  of these companies will be hunted down like common criminals and  accused of "dealing drugs" -- a label that can earn them a red flag on  Interpol (
http://www.naturalnews.com/027750_G...). This is exactly what happened to Greg Caton, who was 
kidnapped from Ecuador by the FDA after manufacturing and selling anti-cancer salves that actually worked quite well to eliminate skin cancer tumors.
Caton's  listing on Interpol said he was wanted for "drugs, related crimes,  fraud." That's the official Interpol listing. What drugs? The skin  cancer salves. What fraud? The "fraud" of selling anti-cancer products.  What "related crimes?" The "crime" of refusing to bow down to the FDA's  outrageous censorship and tyranny.
In this way, the FDA can simply 
fabricate  fictitious accusations against sellers of nutrients and herbs, then use  either U.S. marshals to arrest them at gunpoint in the USA, or invoke  Interpol to have them kidnapped from other countries, in complete  violation of expatriation agreements between nations.
The FDA now seeks to utterly destroy the nutritional supplements industry
Remember, this is 
the FDA's "end game" strategy  to utterly destroy the supplements industry and thereby hand Big Pharma  a complete monopoly over nearly all forms of medicine in the USA. If  this regulation is put into practice, it would cause:
• The complete wipeout of nearly all nutritional supplement companies in the USA.
• The bankruptcy of most health food stores and vitamin retailers, including online retailers.
• A loss of 
millions of jobs  currently supported by the supplements industry. How does this come to  millions of jobs? Add up all the jobs related to the importing,  manufacturing and transportation of nutritional supplements and  superfoods. Include all the jobs related to marketing, advertising,  promoting, distributing and publicizing these supplements. Then include  all the jobs of workers in health food stores, fulfillment centers and  supplement formulators. On top of that, you have all the jobs which are 
supported  by successful nutritional supplement companies, including accounting,  legal, graphic design and technology jobs. The Natural Products  Foundation conservatively says that dietary supplements contribute $61  billion to the U.S. economy and support 
450,000 jobs (
http://naturalproductsfoundation.or...). The FDA's new regulations, however, impact not just dietary supplements but also 
superfoods and 
functional foods  which are part of an even larger market. In all, millions of jobs will  be impacted by the FDA's proposed new regulations. In addition, 
nutritional supplements boost job performance  across all industries because they help employees work better and  reduce sick days. So removing their access to these supplements will 
suppress the productivity of workers across ALL industries. This is one of the ways in which these proposed new regulations could destroy 
millions of jobs across the U.S. economy.
•  Skyrocketing rates of chronic degenerative diseases such as cancer,  heart disease, diabetes and Alzheimer's disease, because nutritional  supplements are practically the only thing keeping these diseases in  check right now.
• A worsening of infectious disease and viral  outbreaks due to weakened immune systems across the U.S. population.  (The CDC will respond by saying we need "more vaccines!")
• Huge increases in 
health care costs due to more patients having more disease and yet having fewer alternatives available for preventing or treating that disease.
The end of the supplements industry would spell the end of America
Because of these reasons, I believe this FDA regulation, if fully enforced, would 
destroy what remains of America's economy  and, within just a few years, cause a total collapse of the health care  system which is already burdened under a rising wave of degenerative  disease (diabetes rates have doubled in just one generation, thanks to  the utter failure of western medicine).
In this proposed FDA regulation, I believe we are looking at a 
deliberate effort to destroy America,  engineered by the unelected criminals and tyrants who run the FDA and  answer to no one. They are writing their own new laws, in essence, with  zero oversight from Congress and no responsibility whatsoever to the  People they are supposed to serve. This is what happens when we allow 
runaway Big Government to trash our economies, mandate failed health care treatments (Obamacare) and nullify the U.S. Constitution.
Obama says he is not engaged in a war against Libya (yeah, right!), but it's clear the FDA has 
declared war on the American people.
And where does the FDA even claim it has the right to deny the use of dietary ingredients? 
The Commerce Clause,  of course! It's the catch-all clause that Big Government always uses to  claim supreme power over the people. And yet it's all a  misinterpretation of the original intent of the Commerce Clause! The  U.S. Constitution was written 
to LIMIT the power of government in order to protect the People from 
precisely the kind of tyranny being unleashed against us by the FDA.
Where you can read more:
Ralph Fucetola, the 
Vitamin Lawyer, shares his thoughts on this issue at: 
http://www.healthfreedomusa.org/?p=9875
Also, the 
Alliance for Natural Health, which originally broke this story, offers an excellent analysis along with an 
online petition I encourage you to sign:
http://www.anh-usa.org/fda-new-snea...
Alert your local health food stores  about this FDA assault on so-called NDIs. Share this article. Make sure  your friends know the FDA is trying to destroy the supplements  industry.
We must not let them succeed. In fact, I say that in a  just society, we would ask the U.S. Department of Justice to lead a  citizens' march into the FDA offices and 
arrest the criminals there,  charge them with crimes against humanity -- plus fraud, racketeering,  and conspiracy to commit murder -- then hold public trials where all the  evidence against the FDA is made public so that the entire population  can see the full extent of the crimes this agency is committing against  the People of this great nation.
We are not just dealing with bureaucrats here, my friends... we are dealing with 
murderers  who absolutely do not value human life in any way -- and who are  committed to causing more disease, more suffering, and more death as  long as they can protect the profits of the pharmaceutical industry.  These FDA bureaucrats are in the same evil class as Nazi war criminals,  and it's time that we subjected them to the full force of 
common law powered by the People.
The sooner that day comes, the safer our nation will be from tyrants. We are now quite literally fighting for our lives.
Stay tuned to NaturalNews.com for more reporting on this developing issue.
To  further discuss this issue, I am appearing on the Alex Jones show  Thursday, July 7th, at 1pm central time. You can view that interview at 
www.PrisonPlanet.TV
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