Package 11673-233-15

{"route": ["TOPICAL"], "spl_id": "247657b8-246a-ff87-e063-6294a90a2067", "openfda": {"unii": ["15FIX9V2JP", "SOI2LOH54Z"], "spl_set_id": ["f99028fa-a17e-4a84-e053-6294a90a927f"], "manufacturer_name": ["TARGET CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "177 mL in 1 TUBE (11673-233-15)", "package_ndc": "11673-233-15", "marketing_start_date": "20200922"}, {"sample": false, "description": "307.5 mL in 1 BOTTLE (11673-233-40)", "package_ndc": "11673-233-40", "marketing_start_date": "20200922"}], "brand_name": "Target Up and Up SPF 50 Mineral Sunscreen", "product_id": "11673-233_247657b8-246a-ff87-e063-6294a90a2067", "dosage_form": "LOTION", "product_ndc": "11673-233", "generic_name": "Titanium Dioxide, Zinc Oxide", "labeler_name": "TARGET CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Target Up and Up SPF 50 Mineral Sunscreen", "active_ingredients": [{"name": "TITANIUM DIOXIDE", "strength": "30 mg/mL"}, {"name": "ZINC OXIDE", "strength": "150 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200922", "listing_expiration_date": "20261231"}