opalescence sensitivity relief whitening

Generic: potassium nitrate and sodium fluoride

Labeler: ultradent products, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name opalescence sensitivity relief whitening
Generic Name potassium nitrate and sodium fluoride
Labeler ultradent products, inc.
Dosage Form GEL, DENTIFRICE
Routes
DENTAL
Active Ingredients

potassium nitrate 50 mg/g, sodium fluoride 1.1 mg/g

Manufacturer
Ultradent Products, Inc.

Identifiers & Regulatory

Product NDC 51206-308
Product ID 51206-308_43d0f364-2387-9fae-e063-6394a90a4777
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M022
Listing Expiration 2026-12-31
Marketing Start 2015-11-30

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 51206308
Hyphenated Format 51206-308

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 opalescence sensitivity relief whitening (source: ndc)
Generic Name potassium nitrate and sodium fluoride (source: ndc)
Application Number M022 (source: ndc)
Routes
DENTAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/g
  • 1.1 mg/g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (51206-308-01) / 28.35 g in 1 TUBE
  • 1 TUBE in 1 CARTON (51206-308-02) / 133 g in 1 TUBE
  • 3 CARTON in 1 PACKAGE, COMBINATION (51206-308-03) / 1 TUBE in 1 CARTON / 133 g in 1 TUBE
  • 12 CARTON in 1 PACKAGE, COMBINATION (51206-308-04) / 1 TUBE in 1 CARTON / 133 g in 1 TUBE
  • 24 CARTON in 1 PACKAGE, COMBINATION (51206-308-05) / 1 TUBE in 1 CARTON / 28.35 g in 1 TUBE
  • 6 CARTON in 1 PACKAGE, COMBINATION (51206-308-06) / 1 TUBE in 1 CARTON / 133 g in 1 TUBE
source: ndc

Packages (6)

Ingredients (2)

potassium nitrate (50 mg/g) sodium fluoride (1.1 mg/g)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["DENTAL"], "spl_id": "43d0f364-2387-9fae-e063-6394a90a4777", "openfda": {"unii": ["RU45X2JN0Z", "8ZYQ1474W7"], "rxcui": ["1086243"], "spl_set_id": ["b5176a84-76a3-4ad0-a2e2-4997a12da9a5"], "manufacturer_name": ["Ultradent Products, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (51206-308-01)  / 28.35 g in 1 TUBE", "package_ndc": "51206-308-01", "marketing_end_date": "20301013", "marketing_start_date": "20151130"}, {"sample": false, "description": "1 TUBE in 1 CARTON (51206-308-02)  / 133 g in 1 TUBE", "package_ndc": "51206-308-02", "marketing_end_date": "20301013", "marketing_start_date": "20151130"}, {"sample": false, "description": "3 CARTON in 1 PACKAGE, COMBINATION (51206-308-03)  / 1 TUBE in 1 CARTON / 133 g in 1 TUBE", "package_ndc": "51206-308-03", "marketing_end_date": "20301013", "marketing_start_date": "20151130"}, {"sample": false, "description": "12 CARTON in 1 PACKAGE, COMBINATION (51206-308-04)  / 1 TUBE in 1 CARTON / 133 g in 1 TUBE", "package_ndc": "51206-308-04", "marketing_end_date": "20301013", "marketing_start_date": "20151130"}, {"sample": false, "description": "24 CARTON in 1 PACKAGE, COMBINATION (51206-308-05)  / 1 TUBE in 1 CARTON / 28.35 g in 1 TUBE", "package_ndc": "51206-308-05", "marketing_end_date": "20301013", "marketing_start_date": "20151130"}, {"sample": false, "description": "6 CARTON in 1 PACKAGE, COMBINATION (51206-308-06)  / 1 TUBE in 1 CARTON / 133 g in 1 TUBE", "package_ndc": "51206-308-06", "marketing_end_date": "20301013", "marketing_start_date": "20151130"}], "brand_name": "Opalescence Sensitivity Relief Whitening", "product_id": "51206-308_43d0f364-2387-9fae-e063-6394a90a4777", "dosage_form": "GEL, DENTIFRICE", "product_ndc": "51206-308", "generic_name": "Potassium Nitrate and Sodium Fluoride", "labeler_name": "Ultradent Products, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Opalescence Sensitivity Relief Whitening", "active_ingredients": [{"name": "POTASSIUM NITRATE", "strength": "50 mg/g"}, {"name": "SODIUM FLUORIDE", "strength": "1.1 mg/g"}], "application_number": "M022", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20151130", "listing_expiration_date": "20261231"}