April 7, 2026
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0:59Now PlayingRFK Jr. joins Clay & Buck and nails the key difference: FDA requires rigorous pre-market approval and clinical trials for drugs that treat diseases (like heart meds or weight-loss drugs). But dietary supplements and many peptides operate under the 1994 DSHEA law — no mandatory FDA review before hitting the market. Manufacturers handle safety and labeling, with FDA stepping in only if problems arise. Is this framework too loose… or does it protect innovation and consumer choice? Full interview on The Clay Travis & Buck Sexton Show. What do you think — should peptides get easier access or stricter rules? Comment below! #RFKJr #FDA #Supplements #Peptides #MakeAmericaHealthyAgain #ClayAndBuck
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