Package 0135-5029-01
Brand: sensodyne advanced whitening plus
Generic: potassium nitratePackage Facts
Identity
Package NDC
0135-5029-01
Digits Only
0135502901
Product NDC
0135-5029
Description
4 TUBE in 1 CARTON (0135-5029-01) / 184 g in 1 TUBE
Marketing
Marketing Status
Brand
sensodyne advanced whitening plus
Generic
potassium nitrate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1d136fd0-e761-deab-e063-6394a90a2452", "openfda": {"unii": ["RU45X2JN0Z", "8ZYQ1474W7"], "rxcui": ["1086243"], "spl_set_id": ["f757ccdd-b316-4799-a34a-10edbb73da6b"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 TUBE in 1 CARTON (0135-5029-01) / 184 g in 1 TUBE", "package_ndc": "0135-5029-01", "marketing_start_date": "20240712"}], "brand_name": "SENSODYNE Advanced Whitening Plus", "product_id": "0135-5029_1d136fd0-e761-deab-e063-6394a90a2452", "dosage_form": "PASTE", "product_ndc": "0135-5029", "generic_name": "potassium nitrate", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SENSODYNE", "brand_name_suffix": "Advanced Whitening Plus", "active_ingredients": [{"name": "POTASSIUM NITRATE", "strength": "50 mg/g"}, {"name": "SODIUM FLUORIDE", "strength": "1.11 mg/g"}], "application_number": "M022", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240712", "listing_expiration_date": "20261231"}