Of the following laws, which one states that all medication products must have directions for use and appropriate safety warnings?

The FFDCA demands all products to comprise a list of ingredients, directions, and safety warnings. It also states that all drugs must be approved by the FDA before being marketed and used by patients. The FFDCA improved upon the Pure Food and Drug Act by adding the safety requirements that the Pure Food and Drug Act was missing. The Isotretinoin Safety and Risk Management Act of 2004 addresses the need for Risk Evaluation and Mitigation Strategy (REMS) criteria and specific monitoring of patients using medications with potentially serious adverse effects. The PPPA describes the security requirements for medication packaging to prevent children from accessing the medication.