{"adverse_reactions":["ADVERSE REACTIONS"],"clinical_pharmacology":["CLINICAL PHARMACOLOGY"],"contraindications":["CONTRAINDICATIONS"],"description":["DESCRIPTION"],"dosage_and_administration":["DOSAGE & ADMINISTRATION"],"effective_time":"20160413","id":"30627fe3-8721-7254-e054-00144ff88e88","indications_and_usage":["INDICATIONS AND USAGE"],"information_for_patients":["MEDICATION GUIDE"],"openfda":{},"overdosage":["OVERDOSAGE"],"package_label_principal_display_panel":["PRINCIPAL DISPLAY PANEL DICLOFENAC75mg30TABS"],"precautions":["PRECAUTIONS"],"set_id":"30627fe3-8720-7254-e054-00144ff88e88","spl_product_data_elements":["DICLOFENAC SODIUM DECLOFENAC SODIUM DICLOFENAC SODIUM DICLOFENAC LACTOSE MONOHYDRATE CELLULOSE, MICROCRYSTALLINE POVIDONE, UNSPECIFIED METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A POLYETHYLENE GLYCOL, UNSPECIFIED TITANIUM DIOXIDE FERRIC OXIDE YELLOW WATER HYPROMELLOSES FERRIC OXIDE RED CROSCARMELLOSE SODIUM TALC MAGNESIUM STEARATE Light Brown P;75"],"version":"1","warnings":["WARNINGS"]}