Package 0135-0481-01

{"route": ["ORAL"], "spl_id": "4c9ab9d6-fc06-eea3-e063-6394a90a5939", "openfda": {"unii": ["RU45X2JN0Z", "8ZYQ1474W7"], "rxcui": ["1086243"], "spl_set_id": ["a2f9d58b-671b-4427-a971-1fceff5f2323"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (0135-0481-01)  / 96.4 g in 1 TUBE", "package_ndc": "0135-0481-01", "marketing_start_date": "20200106"}, {"sample": false, "description": "2 TUBE in 1 CARTON (0135-0481-02)  / 96.4 g in 1 TUBE", "package_ndc": "0135-0481-02", "marketing_start_date": "20200106"}, {"sample": false, "description": "1 TUBE in 1 CARTON (0135-0481-04)  / 65 g in 1 TUBE", "package_ndc": "0135-0481-04", "marketing_start_date": "20251201"}], "brand_name": "SENSODYNE PRONAMEL Intensive Enamel Repair Whitening", "product_id": "0135-0481_4c9ab9d6-fc06-eea3-e063-6394a90a5939", "dosage_form": "PASTE", "product_ndc": "0135-0481", "generic_name": "potassium nitrate and sodium fluoride", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SENSODYNE PRONAMEL", "brand_name_suffix": "Intensive Enamel Repair Whitening", "active_ingredients": [{"name": "POTASSIUM NITRATE", "strength": "50 mg/g"}, {"name": "SODIUM FLUORIDE", "strength": "1.15 mg/g"}], "application_number": "M022", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200106", "listing_expiration_date": "20271231"}