What is Consumer Medication Information mandated by?

Consumer Medication Information (CMI) is mandated primarily by FDA regulations. The FDA has established requirements for the provision of CMI to ensure that patients receive clear and understandable information about their medications. This requirement is part of the agency's effort to enhance medication safety and improve patient education regarding the proper use of prescription drugs. The information provided typically includes details about the medication’s purpose, dosage, side effects, and precautions.

While state pharmacy boards may have their own regulations that also demand the provision of patient information, these rules are generally based on or complement the federal requirements set by the FDA. Manufacturer guidelines and healthcare organizations can provide additional resources or templates for CMI, but the foundational mandate for consumer medication information is derived from federal law. Thus, recognizing the role of the FDA in this context is crucial for understanding the regulated framework within which pharmacy practice operates.