sensodyne advanced whitening

Generic: potassium nitrate

Labeler: haleon us holdings llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name sensodyne advanced whitening
Generic Name potassium nitrate
Labeler haleon us holdings llc
Dosage Form PASTE
Routes
ORAL
Active Ingredients

potassium nitrate 50 mg/g, sodium fluoride 1.15 mg/g

Manufacturer
Haleon US Holdings LLC

Identifiers & Regulatory

Product NDC 0135-0479
Product ID 0135-0479_12d5e856-2c07-35b2-e063-6294a90a2d3b
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M022
Listing Expiration 2026-12-31
Marketing Start 2020-10-16

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01350479
Hyphenated Format 0135-0479

Supplemental Identifiers

RxCUI
1086243
UNII
RU45X2JN0Z 8ZYQ1474W7

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name sensodyne advanced whitening (source: ndc)
Generic Name potassium nitrate (source: ndc)
Application Number M022 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/g
  • 1.15 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (0135-0479-01) / 184 g in 1 TUBE
  • 4 TUBE in 1 CARTON (0135-0479-02) / 184 g in 1 TUBE
source: ndc

Packages (2)

0135-0479-01 1 TUBE in 1 CARTON (0135-0479-01) / 184 g in 1 TUBE 0135-0479-02 4 TUBE in 1 CARTON (0135-0479-02) / 184 g in 1 TUBE

Ingredients (2)

potassium nitrate (50 mg/g) sodium fluoride (1.15 mg/g)

Linked Drug Pages (1)

SENSODYNE Advanced Whitening ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "12d5e856-2c07-35b2-e063-6294a90a2d3b", "openfda": {"unii": ["RU45X2JN0Z", "8ZYQ1474W7"], "rxcui": ["1086243"], "spl_set_id": ["a06e2549-3c4e-4818-b53e-1dea6828219f"], "manufacturer_name": ["Haleon US Holdings LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (0135-0479-01)  / 184 g in 1 TUBE", "package_ndc": "0135-0479-01", "marketing_start_date": "20201016"}, {"sample": false, "description": "4 TUBE in 1 CARTON (0135-0479-02)  / 184 g in 1 TUBE", "package_ndc": "0135-0479-02", "marketing_start_date": "20230703"}], "brand_name": "SENSODYNE Advanced Whitening", "product_id": "0135-0479_12d5e856-2c07-35b2-e063-6294a90a2d3b", "dosage_form": "PASTE", "product_ndc": "0135-0479", "generic_name": "potassium nitrate", "labeler_name": "Haleon US Holdings LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SENSODYNE", "brand_name_suffix": "Advanced 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": "20201016", "listing_expiration_date": "20261231"}