Package 72043-2269-1

{"route": ["TOPICAL"], "spl_id": "634cafd9-4141-47db-a841-2aa6b4212e48", "openfda": {"upc": ["0390205022694"], "unii": ["4Y5P7MUD51", "SOI2LOH54Z"], "spl_set_id": ["b9b5f3ef-bd38-4147-847a-af79da1d9cd6"], "manufacturer_name": ["CP Skin Health Group, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "48 g in 1 BOTTLE (72043-2269-1)", "package_ndc": "72043-2269-1", "marketing_start_date": "20180110"}, {"sample": false, "description": "2 g in 1 PACKET (72043-2269-2)", "package_ndc": "72043-2269-2", "marketing_start_date": "20220706"}], "brand_name": "EltaMD UV Daily Tinted SPF40", "product_id": "72043-2269_634cafd9-4141-47db-a841-2aa6b4212e48", "dosage_form": "LOTION", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "72043-2269", "generic_name": "zinc oxide and octinoxate sunscreen", "labeler_name": "CP Skin Health Group, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "EltaMD UV Daily Tinted SPF40", "active_ingredients": [{"name": "OCTINOXATE", "strength": "75 g/1000g"}, {"name": "ZINC OXIDE", "strength": "90 g/1000g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20180110", "listing_expiration_date": "20261231"}