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Re: Relacore
That’s because under the DSHEA, dietary supplements are classified as foods and not drugs.The FDA cannot place the burden to prove safety on dietary supplement manufacturers as it does for drug and device makers. However, the FDA has the right to pull a supplement if it poses a significant or unreasonable risk. The FDA couldn't prove this with low doses of ephedra. So dietary supplement manufacturers are allowed to resume selling its whole herb ephedra product with less than 10 mg of naturally occurring ephedrine alkaloids per daily dose.
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