Drugplain

Opalescence Sensitivity Relief Whitening 50 mg/g

Potassium Nitrate and Sodium Fluoride · GEL, DENTIFRICE · Ultradent Products, Inc.

No Recall HistoryCurrently in Shortage
Plain English

Opalescence Sensitivity Relief Whitening is a gel, dentifrice containing potassium nitrate and sodium fluoride at 50 mg/g, taken dental. Manufactured by Ultradent Products, Inc..

Key Facts

Brand Name
Opalescence Sensitivity Relief Whitening
Generic Name
Potassium Nitrate and Sodium Fluoride
NDC Code (Product)
51206-308
Manufacturer
Ultradent Products, Inc.
Strength
50 mg/g
Dosage Form
GEL, DENTIFRICE
Route
DENTAL
Marketing Status
Application #
M022
Marketing Start
11/30/2015

Recall History

No Recall History

Frequently Asked Questions

What is Opalescence Sensitivity Relief Whitening used for?

Opalescence Sensitivity Relief Whitening contains Potassium Nitrate and Sodium Fluoride. It is a gel, dentifrice taken dental. Consult your doctor for specific uses.

Is Opalescence Sensitivity Relief Whitening a controlled substance?

Opalescence Sensitivity Relief Whitening is not classified as a controlled substance by the DEA.

What is the generic name for Opalescence Sensitivity Relief Whitening?

The generic name for Opalescence Sensitivity Relief Whitening is Potassium Nitrate and Sodium Fluoride. There are 12 other brand versions of Potassium Nitrate and Sodium Fluoride.

What is the NDC code for Opalescence Sensitivity Relief Whitening 50 mg/g?

The NDC (National Drug Code) for Opalescence Sensitivity Relief Whitening 50 mg/g is 51206-308, listed by Ultradent Products, Inc..