Sensodyne Cavity and Sensitivity 50 mg/g
potassium nitrate, sodium fluoride · PASTE, DENTIFRICE · Haleon US Holdings LLC
Sensodyne Cavity and Sensitivity is a paste, dentifrice containing potassium nitrate, sodium fluoride at 50 mg/g, taken dental. Manufactured by Haleon US Holdings LLC.
Key Facts
- Brand Name
- Sensodyne Cavity and Sensitivity
- Generic Name
- potassium nitrate, sodium fluoride
- NDC Code (Product)
0135-4032- Manufacturer
- Haleon US Holdings LLC
- Strength
- 50 mg/g
- Dosage Form
- PASTE, DENTIFRICE
- Route
- DENTAL
- Marketing Status
- Application #
- M021
- Marketing Start
- 12/15/2025
Recall History
No Recall HistorySide Effects Reported to FDA
FDA FAERS database · These are reported events, not confirmed side effects
Frequently Asked Questions
What is Sensodyne Cavity and Sensitivity used for?
Sensodyne Cavity and Sensitivity contains potassium nitrate, sodium fluoride. It is a paste, dentifrice taken dental. Consult your doctor for specific uses.
Is Sensodyne Cavity and Sensitivity a controlled substance?
Sensodyne Cavity and Sensitivity is not classified as a controlled substance by the DEA.
What is the generic name for Sensodyne Cavity and Sensitivity?
The generic name for Sensodyne Cavity and Sensitivity is potassium nitrate, sodium fluoride. There are 12 other brand versions of potassium nitrate, sodium fluoride.
What is the NDC code for Sensodyne Cavity and Sensitivity 50 mg/g?
The NDC (National Drug Code) for Sensodyne Cavity and Sensitivity 50 mg/g is 0135-4032, 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)