Package 0135-0811-02

{"route": ["ORAL"], "spl_id": "4124888c-4bab-f7b5-e063-6394a90a7532", "openfda": {"unii": ["RU45X2JN0Z", "8ZYQ1474W7"], "rxcui": ["1086243"], "spl_set_id": ["e8a62f24-1db6-45fb-b6e1-5e57103f82bc"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (0135-0811-02)  / 96.4 g in 1 TUBE", "package_ndc": "0135-0811-02", "marketing_start_date": "20250106"}, {"sample": false, "description": "1 TUBE in 1 CARTON (0135-0811-03)  / 65.2 g in 1 TUBE", "package_ndc": "0135-0811-03", "marketing_start_date": "20250106"}, {"sample": false, "description": "2 TUBE in 1 CARTON (0135-0811-23)  / 96.4 g in 1 TUBE", "package_ndc": "0135-0811-23", "marketing_start_date": "20251201"}], "brand_name": "Sensodyne Pronamel Clinical Enamel Strength Whitening Action", "product_id": "0135-0811_4124888c-4bab-f7b5-e063-6394a90a7532", "dosage_form": "PASTE", "product_ndc": "0135-0811", "generic_name": "potassium nitrate, sodium fluoride", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sensodyne Pronamel", "brand_name_suffix": "Clinical Enamel Strength Whitening Action", "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": "20250106", "listing_expiration_date": "20261231"}