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Zdrowie i gospodarka · 03/09/2004

FDA Delays Implementation Date for Over-the-Counter Human Drug Labeling Requirements

The Food and Drug Administration (FDA) is delaying the implementation date for certain over-the-counter (OTC) human drugs due to an upcoming proposal to modify labeling requirements for OTC sunscreen products, pending the outcome of the proposed rulemaking.

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