Package 51206-311-02

{"route": ["DENTAL"], "spl_id": "37cb8c52-923b-ff47-e063-6294a90ab925", "openfda": {"unii": ["RU45X2JN0Z", "8ZYQ1474W7"], "rxcui": ["1086243"], "spl_set_id": ["5ffc0d14-0290-47bb-90e5-90a25a5acc28"], "manufacturer_name": ["Ultradent Products, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (51206-311-01)  / 133 g in 1 TUBE", "package_ndc": "51206-311-01", "marketing_end_date": "20291015", "marketing_start_date": "20231119"}, {"sample": false, "description": "3 CARTON in 1 PACKAGE, COMBINATION (51206-311-02)  / 1 TUBE in 1 CARTON / 133 g in 1 TUBE", "package_ndc": "51206-311-02", "marketing_end_date": "20291015", "marketing_start_date": "20231119"}], "brand_name": "Opal by Opalescence Sensitivity", "product_id": "51206-311_37cb8c52-923b-ff47-e063-6294a90ab925", "dosage_form": "GEL, DENTIFRICE", "product_ndc": "51206-311", "generic_name": "Potassium Nitrate and Sodium Fluoride", "labeler_name": "Ultradent Products, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Opal by Opalescence Sensitivity", "active_ingredients": [{"name": "POTASSIUM NITRATE", "strength": "50 mg/g"}, {"name": "SODIUM FLUORIDE", "strength": "1.1 mg/g"}], "application_number": "M022", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20231119", "listing_expiration_date": "20261231"}