Package 50090-6172-0

{"route": ["TOPICAL"], "spl_id": "8ccae7c4-e443-4cec-a31d-764334293b65", "openfda": {"unii": ["89Y4M234ES", "057Y626693", "19371312D4", "88AYB867L5"], "rxcui": ["1359350"], "spl_set_id": ["01131ba6-6d5b-4710-bec3-ba1769c08c79"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "36 TUBE in 1 CASE (50090-6172-0)  / 28.4 g in 1 TUBE", "package_ndc": "50090-6172-0", "marketing_end_date": "20270831", "marketing_start_date": "20221014"}], "brand_name": "SUNMARK TRIPLE ANTIBIOTIC PLUS PAIN RELIEF", "product_id": "50090-6172_8ccae7c4-e443-4cec-a31d-764334293b65", "dosage_form": "OINTMENT", "pharm_class": ["Aminoglycoside Antibacterial [EPC]", "Aminoglycosides [CS]", "Decreased Cell Wall Synthesis & Repair [PE]", "Polymyxin-class Antibacterial [EPC]", "Polymyxins [CS]"], "product_ndc": "50090-6172", "generic_name": "polymyxin B sulfate, bacitracin zinc, neomycin sulfate, and pramoxine hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SUNMARK TRIPLE ANTIBIOTIC PLUS PAIN RELIEF", "active_ingredients": [{"name": "BACITRACIN ZINC", "strength": "500 [iU]/g"}, {"name": "NEOMYCIN SULFATE", "strength": "3.5 mg/g"}, {"name": "POLYMYXIN B SULFATE", "strength": "10000 [iU]/g"}, {"name": "PRAMOXINE HYDROCHLORIDE", "strength": "10 mg/g"}], "application_number": "M004", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20270831", "marketing_start_date": "20120331"}