Drugplain

Sensodyne Clinical White Enamel Strengthening 50 mg/g

Potassium nitrate, Sodium fluoride · PASTE · Haleon US Holdings LLC

No Recall HistoryCurrently in Shortage
Plain English

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 History

Frequently 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.