Package 72043-2920-2

{"route": ["TOPICAL"], "spl_id": "79386a40-776e-47d1-8909-88776673d1a9", "openfda": {"upc": ["0827854015291"], "unii": ["4Y5P7MUD51", "SOI2LOH54Z"], "spl_set_id": ["c12fa9a4-d7e5-46bf-9bfb-1cbbaa73b450"], "manufacturer_name": ["CP Skin Health Group, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 g in 1 BOTTLE (72043-2920-1)", "package_ndc": "72043-2920-1", "marketing_start_date": "20240509"}, {"sample": false, "description": "2 g in 1 PACKET (72043-2920-2)", "package_ndc": "72043-2920-2", "marketing_start_date": "20240509"}], "brand_name": "UV Daily Deep Tint", "product_id": "72043-2920_79386a40-776e-47d1-8909-88776673d1a9", "dosage_form": "LOTION", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "72043-2920", "generic_name": "octinoxate, zinc oxide sunscreen", "labeler_name": "CP Skin Health Group, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "UV Daily Deep Tint", "active_ingredients": [{"name": "OCTINOXATE", "strength": "750 g/1000g"}, {"name": "ZINC OXIDE", "strength": "900 g/1000g"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240509", "listing_expiration_date": "20261231"}