Package 10237-669-09

{"route": ["DENTAL"], "spl_id": "45bc024f-5151-201e-e063-6294a90a634f", "openfda": {"unii": ["RU45X2JN0Z", "8ZYQ1474W7"], "rxcui": ["1038929"], "spl_set_id": ["935172db-d78f-0c69-e053-2a95a90a0b69"], "manufacturer_name": ["Church & Dwight Co., Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (10237-669-09)  / 25 g in 1 TUBE", "package_ndc": "10237-669-09", "marketing_start_date": "20190215"}, {"sample": false, "description": "1 TUBE in 1 CARTON (10237-669-45)  / 127 g in 1 TUBE", "package_ndc": "10237-669-45", "marketing_start_date": "20171016"}], "brand_name": "Sensitive Teeth and Gums", "product_id": "10237-669_45bc024f-5151-201e-e063-6294a90a634f", "dosage_form": "PASTE, DENTIFRICE", "product_ndc": "10237-669", "generic_name": "Potassium Nitrate, Sodium Fluoride", "labeler_name": "Church & Dwight Co., Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sensitive Teeth and Gums", "active_ingredients": [{"name": "POTASSIUM NITRATE", "strength": "50 mg/g"}, {"name": "SODIUM FLUORIDE", "strength": "2.43 mg/g"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20171016", "listing_expiration_date": "20261231"}