NDC 51206-315 – Opalescence Whitening Sensitivity Relief

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

Human Otc Drug

Product NDC51206-315

Product details

Brand name
Opalescence Whitening Sensitivity Relief
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
October 8, 2025
Marketing end
December 31, 2030

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
51206-315-011 TUBE in 1 CARTON (51206-315-01) / 133 g in 1 TUBEOct 8, 2025
51206-315-0212 CARTON in 1 PACKAGE, COMBINATION (51206-315-02) / 1 TUBE in 1 CARTON / 133 g in 1 TUBEOct 8, 2025
51206-315-031 TUBE in 1 CARTON (51206-315-03) / 28 g in 1 TUBEOct 8, 2025
51206-315-0424 CARTON in 1 PACKAGE, COMBINATION (51206-315-04) / 1 TUBE in 1 CARTON / 28 g in 1 TUBEOct 8, 2025
51206-315-0548 CARTON in 1 PACKAGE, COMBINATION (51206-315-05) / 1 TUBE in 1 CARTON / 28 g in 1 TUBEOct 8, 2025