Package 69367-318-01

{"route": ["DENTAL"], "spl_id": "0c9c8462-f962-4615-8649-dea8e1ecb498", "openfda": {"unii": ["RU45X2JN0Z", "8ZYQ1474W7"], "rxcui": ["637365"], "spl_set_id": ["7a051d80-879d-4995-96ef-77b60dad26b7"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (69367-318-01)  / 100 mL in 1 TUBE", "package_ndc": "69367-318-01", "marketing_start_date": "20220615"}], "brand_name": "Sodium Fluoride and Potassium Nitrate", "product_id": "69367-318_0c9c8462-f962-4615-8649-dea8e1ecb498", "dosage_form": "GEL", "product_ndc": "69367-318", "generic_name": "Sodium Fluoride and Potassium Nitrate", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Fluoride and Potassium Nitrate", "active_ingredients": [{"name": "POTASSIUM NITRATE", "strength": "57.5 mg/mL"}, {"name": "SODIUM FLUORIDE", "strength": "5.8 mg/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20220615", "listing_expiration_date": "20261231"}