Package 51672-2089-2

{"route": ["TOPICAL"], "spl_id": "38e51539-2525-fa76-e063-6294a90a6b0a", "openfda": {"unii": ["TC2D6JAD40", "FM5526K07A"], "rxcui": ["1087026"], "spl_set_id": ["c89e3de8-7d71-485c-8fc5-2832d6024f16"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (51672-2089-2)  / 28.4 g in 1 TUBE", "package_ndc": "51672-2089-2", "marketing_start_date": "20050920"}], "brand_name": "Diphenhydramine Hydrochloride and Zinc Acetate", "product_id": "51672-2089_38e51539-2525-fa76-e063-6294a90a6b0a", "dosage_form": "CREAM", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "51672-2089", "generic_name": "Diphenhydramine Hydrochloride and Zinc Acetate", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Diphenhydramine Hydrochloride and Zinc Acetate", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "20 mg/g"}, {"name": "ZINC ACETATE", "strength": "1 mg/g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20050920", "listing_expiration_date": "20261231"}