Package 72220-003-02

{"route": ["TOPICAL"], "spl_id": "30877734-91d7-34c8-e063-6294a90a0e64", "openfda": {"unii": ["V06SV4M95S", "4X49Y0596W", "5A68WGF6WM", "SOI2LOH54Z"], "spl_set_id": ["3087771e-2ab8-2198-e063-6294a90a37d4"], "manufacturer_name": ["SKINIDEA CO., LTD"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (72220-003-02)  / 40 mL in 1 TUBE (72220-003-01)", "package_ndc": "72220-003-02", "marketing_start_date": "20250301"}], "brand_name": "MDP UV BIO SUNSCREEN", "product_id": "72220-003_30877734-91d7-34c8-e063-6294a90a0e64", "dosage_form": "CREAM", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "72220-003", "generic_name": "ZINC OXIDE, HOMOSALATE, OCTOCRYLENE, OCTISALATE", "labeler_name": "SKINIDEA CO., LTD", "product_type": "HUMAN OTC DRUG", "brand_name_base": "MDP UV BIO SUNSCREEN", "active_ingredients": [{"name": "HOMOSALATE", "strength": "60 mg/mL"}, {"name": "OCTISALATE", "strength": "45 mg/mL"}, {"name": "OCTOCRYLENE", "strength": "50 mg/mL"}, {"name": "ZINC OXIDE", "strength": "103.8 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250301", "listing_expiration_date": "20261231"}