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Farnsworth goes on to state the fda final rules on labeling statements, in my opinion, were not helpful to industry as to how to craft truthful and non misleading health claims. Friedman, md, lead deputy commissioner of the fda to inform you thusly cholestin does not contain a prescription or regulated drug. On december 15, 1997 he sent a letter to michael a.

Hammell, legislative advocate, iahf, , your proposed rule to limit manufacturers ability to properly inform the american public on the health benefits of dietary supplements flies in the face of sound public health policy, and constitutes nothing more than a crass and despicable effort to protect the interests of multinational pharmaceutical giants whose profits you protect at the expense of the american public. Regulations on statements made for dietary supplements concerning the effect of the product on the structure or function of the body proposed rule and dietary supplements comments on report of the commission on dietary supplement labels notice submit written comments to dockets management branch (hfa-305) fda 200 c. Sw, washington dc 20204, this info provided courtesy john c.

It contains mevolin, which is chemically distinct from lovastatin (mevacor), the latter being a prescription drug. Your bias against the use of dietary supplements is glaringly apparent in the case of fda v pharmanex, manufacturers of a product called cholestin, an extract of red rice yeast, which you (and merck) falsely maintain contains the prescription drug lovastatin which is sold by merck under the trade name mevacor. We told you to keep your hands off our supplements, and we mean it! I am ccing this to my congressman to request that he cosponsor hr 2868 the consumer health free speech act, which removes food from the current, overly broad statutory definition of drug because foods are of the despicable efforts of the eu funded escop at university of exeter in the uk to attempt to force the global harmonization of laws governing the manufacture and sale of herbal products, just as we are also by the german codex proposal to restrict our access to only rda levels of vitamins & minerals! Iahf has exposed the whole scam at , especially the anpr in the july 7, 1997 federal register (vol.

Research professor in pharmacognosy and senior university scholar at university of illinois. He is a former member of the presidentially appointed commission on dietary supplement labels. .

Farnsworth went on to say it seems to me that having a mild to moderately elevated cholesterol level being lowered is a clear structure function claim as opposed to a statement that lowering cholesterol may prevent atherosclerosis. This fact, in combination with a knowledge that the fermented red rice product has been used as a food or dietary supplement both in china and the united states for many years, in my opinion makes the product a dietary supplement as defined in dshea. ). Cdsl took two years to study this matter, yet it is painfully evident that in your zeal to harmonize american food and drug laws to eec 6565 (an eu directive which turns all dietary supplements into drugs) that you choose to utterly ignore this presidentially appointed commission, and further waste our tax dollars attacking pharmanex due to the revolving door between the fda and such pharmaceutical giants as merck.

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Your bias against the use of dietary supplements is glaringly apparent in the case of fda v pharmanex, manufacturers of a product called cholestin, an extract of red rice yeast, which you (and merck) falsely maintain contains the prescription drug lovastatin which is sold by merck under the trade name mevacor. Friedman, md, lead deputy commissioner of the fda to inform you thusly cholestin does not contain a prescription or regulated drug. Regulations on statements made for dietary supplements concerning the effect of the product on the structure or function of the body proposed rule and dietary supplements comments on report of the commission on dietary supplement labels notice submit written comments to dockets management branch (hfa-305) fda 200 c.

). Farnsworth went on to say it seems to me that having a mild to moderately elevated cholesterol level being lowered is a clear structure function claim as opposed to a statement that lowering cholesterol may prevent atherosclerosis. On december 15, 1997 he sent a letter to michael a.

Sw, washington dc 20204, this info provided courtesy john c. We told you to keep your hands off our supplements, and we mean it! I am ccing this to my congressman to request that he cosponsor hr 2868 the consumer health free speech act, which removes food from the current, overly broad statutory definition of drug because foods are of the despicable efforts of the eu funded escop at university of exeter in the uk to attempt to force the global harmonization of laws governing the manufacture and sale of herbal products, just as we are also by the german codex proposal to restrict our access to only rda levels of vitamins & minerals! Iahf has exposed the whole scam at , especially the anpr in the july 7, 1997 federal register (vol. He is a former member of the presidentially appointed commission on dietary supplement labels.

Research professor in pharmacognosy and senior university scholar at university of illinois. . Hammell, legislative advocate, iahf, , your proposed rule to limit manufacturers ability to properly inform the american public on the health benefits of dietary supplements flies in the face of sound public health policy, and constitutes nothing more than a crass and despicable effort to protect the interests of multinational pharmaceutical giants whose profits you protect at the expense of the american public.

Farnsworth goes on to state the fda final rules on labeling statements, in my opinion, were not helpful to industry as to how to craft truthful and non misleading health claims. This fact, in combination with a knowledge that the fermented red rice product has been used as a food or dietary supplement both in china and the united states for many years, in my opinion makes the product a dietary supplement as defined in dshea. Cdsl took two years to study this matter, yet it is painfully evident that in your zeal to harmonize american food and drug laws to eec 6565 (an eu directive which turns all dietary supplements into drugs) that you choose to utterly ignore this presidentially appointed commission, and further waste our tax dollars attacking pharmanex due to the revolving door between the fda and such pharmaceutical giants as merck. It contains mevolin, which is chemically distinct from lovastatin (mevacor), the latter being a prescription drug.

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    ). It contains mevolin, which is chemically distinct from lovastatin (mevacor), the latter being a prescription drug. Farnsworth goes on to state the fda final rules on labeling statements, in my opinion, were not helpful to industry as to how to craft truthful and non misleading health claims

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    Your bias against the use of dietary supplements is glaringly apparent in the case of fda v pharmanex, manufacturers of a product called cholestin, an extract of red rice yeast, which you (and merck) falsely maintain contains the prescription drug lovastatin which is sold by merck under the trade name mevacor

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    . Hammell, legislative advocate, iahf, , your proposed rule to limit manufacturers ability to properly inform the american public on the health benefits of dietary supplements flies in the face of sound public health policy, and constitutes nothing more than a crass and despicable effort to protect the interests of multinational pharmaceutical giants whose profits you protect at the expense of the american public

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    Your bias against the use of dietary supplements is glaringly apparent in the case of fda v pharmanex, manufacturers of a product called cholestin, an extract of red rice yeast, which you (and merck) falsely maintain contains the prescription drug lovastatin which is sold by merck under the trade name mevacor