Opalescence Whitening Sensitivity Relief 50 mg/g
Potassium Nitrate and Sodium Fluoride · GEL, DENTIFRICE · Ultradent Products, Inc.
Opalescence Whitening Sensitivity Relief 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 Whitening Sensitivity Relief
- Generic Name
- Potassium Nitrate and Sodium Fluoride
- NDC Code (Product)
51206-315- Manufacturer
- Ultradent Products, Inc.
- Strength
- 50 mg/g
- Dosage Form
- GEL, DENTIFRICE
- Route
- DENTAL
- Marketing Status
- Application #
- M022
- Marketing Start
- 10/08/2025
Recall History
No Recall HistoryFrequently Asked Questions
What is Opalescence Whitening Sensitivity Relief used for?
Opalescence Whitening Sensitivity Relief contains Potassium Nitrate and Sodium Fluoride. It is a gel, dentifrice taken dental. Consult your doctor for specific uses.
Is Opalescence Whitening Sensitivity Relief a controlled substance?
Opalescence Whitening Sensitivity Relief is not classified as a controlled substance by the DEA.
What is the generic name for Opalescence Whitening Sensitivity Relief?
The generic name for Opalescence Whitening Sensitivity Relief 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 Whitening Sensitivity Relief 50 mg/g?
The NDC (National Drug Code) for Opalescence Whitening Sensitivity Relief 50 mg/g is 51206-315, listed by Ultradent Products, Inc..
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Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)