To amend the Federal Food, Drug, and Cosmetic Act to require that manufacturers of dietary supplements submit to the Food and Drug Administration reports on adverse experiences with dietary supplements, and for other purposes.
Sponsor: Sen Durbin, Richard J. [IL] (introduced 3/26/2003)
Cosponsors: 4
Latest Major Action: 3/26/2003 Referred to Senate committee.
Status: Read twice and referred to the Committee on Health, Education, Labor, and Pensions.
TAKE ACTION! Congress is writing the WRONG prescription for health. S. 722 seriously threatens DSHEA and your right to use safe, natural dietary supplements. Click here to send a message to your Senators today!