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Zdrowie i gospodarka · 23/07/2013

FDA Requests Public Comment on Proposed Format and Content Requirements for Over-the-Counter Drug Product Labeling

The Food and Drug Administration (FDA) is seeking public input on proposed standardized format and content requirements for labeling of over-the-counter (OTC) drug products, as mandated by the Paperwork Reduction Act of 1995.

Source: Federal Register — Food and Drug AdministrationOpen original release →