NDC 51206-308 – Opalescence Sensitivity Relief Whitening

Potassium Nitrate 50 mg/g; Sodium Fluoride 1.1 mg/g · Gel, Dentifrice · Dental

Human Otc Drug

Product NDC51206-308

Product details

Brand name
Opalescence Sensitivity Relief Whitening
Generic name
Potassium Nitrate and Sodium Fluoride
Labeler
Ultradent Products, Inc.
Dosage form
Gel, Dentifrice
Route
Dental
Marketing category
OTC MONOGRAPH DRUG · M022
Marketed since
November 30, 2015
Marketing end
October 13, 2030

Active ingredients

Uses, dosage, side effects and warnings for Opalescence Sensitivity Relief Whitening →

Package NDC codes (6)

Package NDCDescriptionSince
51206-308-011 TUBE in 1 CARTON (51206-308-01) / 28.35 g in 1 TUBENov 30, 2015
51206-308-021 TUBE in 1 CARTON (51206-308-02) / 133 g in 1 TUBENov 30, 2015
51206-308-033 CARTON in 1 PACKAGE, COMBINATION (51206-308-03) / 1 TUBE in 1 CARTON / 133 g in 1 TUBENov 30, 2015
51206-308-0412 CARTON in 1 PACKAGE, COMBINATION (51206-308-04) / 1 TUBE in 1 CARTON / 133 g in 1 TUBENov 30, 2015
51206-308-0524 CARTON in 1 PACKAGE, COMBINATION (51206-308-05) / 1 TUBE in 1 CARTON / 28.35 g in 1 TUBENov 30, 2015
51206-308-066 CARTON in 1 PACKAGE, COMBINATION (51206-308-06) / 1 TUBE in 1 CARTON / 133 g in 1 TUBENov 30, 2015