Package 59208-002-05

{"route": ["TOPICAL"], "spl_id": "24b2e848-505d-3cf9-e063-6394a90a16d7", "openfda": {"unii": ["F5UM2KM3W7", "V13007Z41A"], "rxcui": ["1431682", "1431687"], "spl_set_id": ["89081ef8-9721-a476-e053-2995a90ae0de"], "manufacturer_name": ["Laboratorios Liomont, S.A. de C.V."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (59208-002-04)  / 4 g in 1 TUBE", "package_ndc": "59208-002-04", "marketing_start_date": "20190501"}, {"sample": false, "description": "1 TUBE in 1 CONTAINER (59208-002-05)  / 4 g in 1 TUBE", "package_ndc": "59208-002-05", "marketing_start_date": "20190501"}], "brand_name": "CICLOFERON", "product_id": "59208-002_24b2e848-505d-3cf9-e063-6394a90a16d7", "dosage_form": "GEL", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "59208-002", "generic_name": "benzalkonium chloride and lidocaine hydrochloride", "labeler_name": "Laboratorios Liomont, S.A. de C.V.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "CICLOFERON", "active_ingredients": [{"name": "BENZALKONIUM CHLORIDE", "strength": "1.3 mg/g"}, {"name": "LIDOCAINE HYDROCHLORIDE", "strength": "20 mg/g"}], "application_number": "M003", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190501", "listing_expiration_date": "20261231"}