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The Federal Trade Commission should continue monitoring restraints of trade in the generic drug industry.
Efforts to expedite FDA approval processes should ensure that patient safety remains paramount.
Federal and state policymakers should ensure that practices do not unfairly exclude competition in the prescription drug market.
Congress should fund a systematic review of the safety and efficacy of the most common dietary supplements.
The FDA should require supplement manufacturers’ labels to include possible supplement interactions with commonly prescribed prescription drugs.
Federal agencies that oversee food labeling and advertising should adopt consistent standards.
Food labels should be written in clear, plain, understandable language and printed in legible type size, font, and color.
Federal agencies should take strong action against misleading and deceptive labeling practices and advertisements.