Package 0135-4032-01

Brand: sensodyne cavity and sensitivity

Generic: potassium nitrate, sodium fluoride
NDC Package

Package Facts

Identity

Package NDC 0135-4032-01
Digits Only 0135403201
Product NDC 0135-4032
Description

1 TUBE in 1 CARTON (0135-4032-01) / 77 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2025-12-15
Brand sensodyne cavity and sensitivity
Generic potassium nitrate, sodium fluoride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["DENTAL"], "spl_id": "445ed08a-b479-1982-e063-6394a90a6cc3", "openfda": {"unii": ["RU45X2JN0Z", "8ZYQ1474W7"], "rxcui": ["1086243"], "spl_set_id": ["d002074b-0580-4247-b3c7-121b8c098697"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (0135-4032-01)  / 77 g in 1 TUBE", "package_ndc": "0135-4032-01", "marketing_start_date": "20251215"}], "brand_name": "Sensodyne Cavity and Sensitivity", "product_id": "0135-4032_445ed08a-b479-1982-e063-6394a90a6cc3", "dosage_form": "PASTE, DENTIFRICE", "product_ndc": "0135-4032", "generic_name": "potassium nitrate, sodium fluoride", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sensodyne", "brand_name_suffix": "Cavity and Sensitivity", "active_ingredients": [{"name": "POTASSIUM NITRATE", "strength": "50 mg/g"}, {"name": "SODIUM FLUORIDE", "strength": "1.5 mg/g"}], "application_number": "M021", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20251215", "listing_expiration_date": "20261231"}