Package 0135-5030-01

Brand: sensodyne pronamel gentle whitening advanced plus

Generic: potassium nitrate, sodium fluoride
NDC Package

Package Facts

Identity

Package NDC 0135-5030-01
Digits Only 0135503001
Product NDC 0135-5030
Product ID 0135-5030_20d4e774-84c8-0538-e063-6394a90aadf4
Description

4 TUBE in 1 CARTON (0135-5030-01) / 184 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2024-10-01
Brand sensodyne pronamel gentle whitening advanced plus
Generic potassium nitrate, sodium fluoride
Sample Package No

Linked Drug Pages (1)

Sensodyne Pronamel Gentle Whitening Advanced Plus ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "20d4e774-84c8-0538-e063-6394a90aadf4", "openfda": {"unii": ["RU45X2JN0Z", "8ZYQ1474W7"], "rxcui": ["1086243"], "spl_set_id": ["6eb304dd-2a24-4fa0-9d39-71264e88dd16"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "4 TUBE in 1 CARTON (0135-5030-01)  / 184 g in 1 TUBE", "package_ndc": "0135-5030-01", "marketing_start_date": "20241001"}], "brand_name": "Sensodyne Pronamel Gentle Whitening Advanced Plus", "product_id": "0135-5030_20d4e774-84c8-0538-e063-6394a90aadf4", "dosage_form": "PASTE", "product_ndc": "0135-5030", "generic_name": "potassium nitrate, sodium fluoride", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sensodyne", "brand_name_suffix": "Pronamel Gentle Whitening Advanced 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": "20241001", "listing_expiration_date": "20261231"}