Sensodyne Clinical White Enamel Strengthening 50 mg/g
Potassium nitrate, Sodium fluoride · PASTE · Haleon US Holdings LLC
Sensodyne Clinical White Enamel Strengthening is a paste containing potassium nitrate, sodium fluoride at 50 mg/g, taken oral. Manufactured by Haleon US Holdings LLC.
Key Facts
- Brand Name
- Sensodyne Clinical White Enamel Strengthening
- Generic Name
- Potassium nitrate, Sodium fluoride
- NDC Code (Product)
0135-0703- Manufacturer
- Haleon US Holdings LLC
- Strength
- 50 mg/g
- Dosage Form
- PASTE
- Route
- ORAL
- Marketing Status
- Application #
- M022
- Marketing Start
- 01/02/2024
Recall History
No Recall HistoryFrequently Asked Questions
What is Sensodyne Clinical White Enamel Strengthening used for?
Sensodyne Clinical White Enamel Strengthening contains Potassium nitrate, Sodium fluoride. It is a paste taken oral. Consult your doctor for specific uses.
Is Sensodyne Clinical White Enamel Strengthening a controlled substance?
Sensodyne Clinical White Enamel Strengthening is not classified as a controlled substance by the DEA.
What is the generic name for Sensodyne Clinical White Enamel Strengthening?
The generic name for Sensodyne Clinical White Enamel Strengthening is Potassium nitrate, Sodium fluoride. There are 11 other brand versions of Potassium nitrate, Sodium fluoride.
What is the NDC code for Sensodyne Clinical White Enamel Strengthening 50 mg/g?
The NDC (National Drug Code) for Sensodyne Clinical White Enamel Strengthening 50 mg/g is 0135-0703, listed by Haleon US Holdings LLC.
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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)