Package 69968-0459-1

{"route": ["TOPICAL"], "spl_id": "399004db-8df3-c030-e063-6294a90a260b", "openfda": {"upc": ["0312547171403"], "unii": ["TC2D6JAD40", "FM5526K07A"], "rxcui": ["1294589", "1294591"], "spl_set_id": ["309d9be0-e367-429a-a1fa-ab7855477c8a"], "manufacturer_name": ["Kenvue Brands LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 APPLICATOR in 1 CARTON (69968-0459-1)  / 14 mL in 1 APPLICATOR", "package_ndc": "69968-0459-1", "marketing_start_date": "20190601"}], "brand_name": "Benadryl Extra Strength Itch Relief", "product_id": "69968-0459_399004db-8df3-c030-e063-6294a90a260b", "dosage_form": "SOLUTION", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "69968-0459", "generic_name": "DIPHENHYDRAMINE HYDROCHLORIDE and Zinc Acetate", "labeler_name": "Kenvue Brands LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Benadryl Extra Strength Itch Relief", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "20 mg/mL"}, {"name": "ZINC ACETATE", "strength": "1 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190601", "listing_expiration_date": "20261231"}