opalescence sensitivity relief whitening
Generic: potassium nitrate and sodium fluoride
Labeler: ultradent products, inc.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
Active Ingredients
potassium nitrate 50 mg/g, sodium fluoride 1.1 mg/g
Manufacturer
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
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 50 mg/g
- 1.1 mg/g
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
Packages (6)
51206-308-01
1 TUBE in 1 CARTON (51206-308-01) / 28.35 g in 1 TUBE
51206-308-02
1 TUBE in 1 CARTON (51206-308-02) / 133 g in 1 TUBE
51206-308-03
3 CARTON in 1 PACKAGE, COMBINATION (51206-308-03) / 1 TUBE in 1 CARTON / 133 g in 1 TUBE
51206-308-04
12 CARTON in 1 PACKAGE, COMBINATION (51206-308-04) / 1 TUBE in 1 CARTON / 133 g in 1 TUBE
51206-308-05
24 CARTON in 1 PACKAGE, COMBINATION (51206-308-05) / 1 TUBE in 1 CARTON / 28.35 g in 1 TUBE
51206-308-06
6 CARTON in 1 PACKAGE, COMBINATION (51206-308-06) / 1 TUBE in 1 CARTON / 133 g in 1 TUBE
Ingredients (2)
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"}