Food and Drug Administration (FDA) has issued guidance and revisions regarding compounding certain ibuprofen oral suspension products to address the ongoing demand for fever- and pain-reducing medications. The latest guidance revisions provide recommendations for ibuprofen oral suspension products compounded by outsourcing facilities and supplied to state-licensed pharmacies (including those within hospitals and health systems) and applicable federal facilities that dispense the medication to patients for home use following receipt of a valid, patient-specific prescription from a health care provider.