Package 10237-678-12

{"route": ["ORAL"], "spl_id": "88d71cb7-8abf-407d-a74c-f5537497759a", "openfda": {"unii": ["RU45X2JN0Z", "8ZYQ1474W7"], "spl_set_id": ["7b9d9e7d-3844-4d18-ab03-bd0e9dcfccdb"], "manufacturer_name": ["Church & Dwight Co., Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 TUBE in 1 CARTON (10237-678-12)  / 170 g in 1 TUBE", "package_ndc": "10237-678-12", "marketing_start_date": "20240601"}, {"sample": false, "description": "121.9 g in 1 TUBE (10237-678-43)", "package_ndc": "10237-678-43", "marketing_start_date": "20240131"}], "brand_name": "Orajel Sensitivity Relief", "product_id": "10237-678_88d71cb7-8abf-407d-a74c-f5537497759a", "dosage_form": "PASTE, DENTIFRICE", "product_ndc": "10237-678", "generic_name": "Sodium Fluoride and Potassium Nitrate", "labeler_name": "Church & Dwight Co., Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Orajel Sensitivity Relief", "active_ingredients": [{"name": "POTASSIUM NITRATE", "strength": "5 g/100g"}, {"name": "SODIUM FLUORIDE", "strength": ".243 g/100g"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240131", "listing_expiration_date": "20261231"}