{"effective_time":"20250129","id":"2cdbe7df-4c68-9b05-e063-6394a90a4699","openfda":{"brand_name":["Banophen"],"generic_name":["DIPHENHYDRAMINE HCL"],"manufacturer_name":["Health Department, Oklahoma State"],"original_packager_product_ndc":["0904-5551"],"package_ndc":["83112-555-59"],"product_ndc":["83112-555"],"product_type":["HUMAN PRESCRIPTION DRUG"],"route":["ORAL"],"rxcui":["1049630","1092421"],"spl_id":["2cdbe7df-4c68-9b05-e063-6394a90a4699"],"spl_set_id":["2cdbe7df-4c67-9b05-e063-6394a90a4699"],"substance_name":["DIPHENHYDRAMINE HYDROCHLORIDE"],"unii":["TC2D6JAD40"]},"package_label_principal_display_panel":["Diphenhydramine HCl"],"set_id":"2cdbe7df-4c67-9b05-e063-6394a90a4699","spl_product_data_elements":["Banophen Diphenhydramine HCl DIPHENHYDRAMINE HYDROCHLORIDE DIPHENHYDRAMINE 44;329"],"version":"1","when_using":["marked drowsiness may occur avoid alcoholic beverages alcohol, sedatives, and tranquilizers may increase drowsiness use caution when driving a motor vehicle or operating machinery excitability may occur, especially in children"]}