Package 68016-715-01

{"route": ["TOPICAL"], "spl_id": "c6bc1e43-7d2c-460d-9465-b17efe3c50ad", "openfda": {"upc": ["0840986032424"], "unii": ["89Y4M234ES", "057Y626693", "19371312D4", "88AYB867L5"], "rxcui": ["1359350"], "spl_set_id": ["55ef2205-aaf1-4aa4-917f-2b4cfa43b77e"], "manufacturer_name": ["Chain Drug Consortium, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (68016-715-01)  / 28 g in 1 TUBE", "package_ndc": "68016-715-01", "marketing_end_date": "20261231", "marketing_start_date": "20150710"}], "brand_name": "Triple Antibiotic plus Pain Relief Maximum Strength", "product_id": "68016-715_c6bc1e43-7d2c-460d-9465-b17efe3c50ad", "dosage_form": "OINTMENT", "pharm_class": ["Aminoglycoside Antibacterial [EPC]", "Aminoglycosides [CS]", "Decreased Cell Wall Synthesis & Repair [PE]", "Polymyxin-class Antibacterial [EPC]", "Polymyxins [CS]"], "product_ndc": "68016-715", "generic_name": "bacitracin zinc, neomycin sulfate, polymyxin b sulfate and pramoxine hydrochloride", "labeler_name": "Chain Drug Consortium, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Triple Antibiotic plus Pain Relief", "brand_name_suffix": "Maximum Strength", "active_ingredients": [{"name": "BACITRACIN ZINC", "strength": "500 [USP'U]/g"}, {"name": "NEOMYCIN SULFATE", "strength": "3.5 mg/g"}, {"name": "POLYMYXIN B SULFATE", "strength": "10000 [USP'U]/g"}, {"name": "PRAMOXINE HYDROCHLORIDE", "strength": "10 mg/g"}], "application_number": "M004", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20261231", "marketing_start_date": "20150710"}