Opalescence Sensitivity Relief Whitening 50 mg/g
Potassium Nitrate and Sodium Fluoride · GEL, DENTIFRICE · Ultradent Products, Inc.
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 HistoryFrequently 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..
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Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
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