Drugplain

Sensodyne Pronamel Clinical Enamel Strength Fresh Breath 50 mg/g

potassium nitrate, sodium fluoride · PASTE, DENTIFRICE · Haleon US Holdings LLC

No Recall HistoryCurrently in Shortage
Plain English

Sensodyne Pronamel Clinical Enamel Strength Fresh Breath 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 Pronamel Clinical Enamel Strength Fresh Breath
Generic Name
potassium nitrate, sodium fluoride
NDC Code (Product)
0135-7753
Manufacturer
Haleon US Holdings LLC
Strength
50 mg/g
Dosage Form
PASTE, DENTIFRICE
Route
DENTAL
Marketing Status
Application #
M021
Marketing Start
12/01/2025

Recall History

No Recall History

Frequently Asked Questions

What is Sensodyne Pronamel Clinical Enamel Strength Fresh Breath used for?

Sensodyne Pronamel Clinical Enamel Strength Fresh Breath contains potassium nitrate, sodium fluoride. It is a paste, dentifrice taken dental. Consult your doctor for specific uses.

Is Sensodyne Pronamel Clinical Enamel Strength Fresh Breath a controlled substance?

Sensodyne Pronamel Clinical Enamel Strength Fresh Breath is not classified as a controlled substance by the DEA.

What is the generic name for Sensodyne Pronamel Clinical Enamel Strength Fresh Breath?

The generic name for Sensodyne Pronamel Clinical Enamel Strength Fresh Breath is potassium nitrate, sodium fluoride. There are 12 other brand versions of potassium nitrate, sodium fluoride.

What is the NDC code for Sensodyne Pronamel Clinical Enamel Strength Fresh Breath 50 mg/g?

The NDC (National Drug Code) for Sensodyne Pronamel Clinical Enamel Strength Fresh Breath 50 mg/g is 0135-7753, listed by Haleon US Holdings LLC.