Package 68479-291-04

{"route": ["TOPICAL"], "spl_id": "67812343-d9bc-43df-88d2-85adf578604e", "openfda": {"unii": ["SOI2LOH54Z"], "spl_set_id": ["37a7362a-b251-4d3a-a957-65d8f338fa12"], "manufacturer_name": ["Dermalogica, LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (68479-291-02)  / 30 mL in 1 TUBE", "package_ndc": "68479-291-02", "marketing_start_date": "20221201"}, {"sample": false, "description": "59 mL in 1 TUBE (68479-291-04)", "package_ndc": "68479-291-04", "marketing_start_date": "20221201"}, {"sample": false, "description": "5 mL in 1 TUBE (68479-291-05)", "package_ndc": "68479-291-05", "marketing_start_date": "20221201"}], "brand_name": "PORESCREEN SPF40", "product_id": "68479-291_67812343-d9bc-43df-88d2-85adf578604e", "dosage_form": "LOTION", "product_ndc": "68479-291", "generic_name": "Zinc Oxide", "labeler_name": "Dermalogica, LLC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "PORESCREEN SPF40", "active_ingredients": [{"name": "ZINC OXIDE", "strength": "10 mg/100mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20221201", "listing_expiration_date": "20261231"}