Does the FDA make sense?
The Food and Drug Administration is hard to understand.
On the one hand, they’d like to keep Americans from using herbal cures, though all they’ve done is to create a fantasy: It’s okay to market herbs if they’re called "dietary supplements."
On the other hand, the FDA is ignoring a vital need: Testing ALL herbs sold in the U.S. -- either domestic or imported. This is an urgent need. Many packaging companies are producing private-label brands that can be harmful.
Do these U.S. companies care? Apparently not!. Their only goal is to buy cheap -- and nobody can beat the prices of a ‘mountain bandit.’ And if their bulk-shipped herbs contain harmful additives or if the potency is almost non-existent? They don’t seem to care.
On the one hand, they’d like to keep Americans from using herbal cures, though all they’ve done is to create a fantasy: It’s okay to market herbs if they’re called "dietary supplements."
On the other hand, the FDA is ignoring a vital need: Testing ALL herbs sold in the U.S. -- either domestic or imported. This is an urgent need. Many packaging companies are producing private-label brands that can be harmful.
Do these U.S. companies care? Apparently not!. Their only goal is to buy cheap -- and nobody can beat the prices of a ‘mountain bandit.’ And if their bulk-shipped herbs contain harmful additives or if the potency is almost non-existent? They don’t seem to care.
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