AQUAFRESH EXTREME CLEAN WHITENING ACTION 1.13 mg/g
sodium fluoride · PASTE · Haleon US Holdings LLC
AQUAFRESH EXTREME CLEAN WHITENING ACTION is a paste containing sodium fluoride at 1.13 mg/g, taken dental. Manufactured by Haleon US Holdings LLC.
Key Facts
- Brand Name
- AQUAFRESH EXTREME CLEAN WHITENING ACTION
- Generic Name
- sodium fluoride
- NDC Code (Product)
0135-0234- Manufacturer
- Haleon US Holdings LLC
- Strength
- 1.13 mg/g
- Dosage Form
- PASTE
- Route
- DENTAL
- Marketing Status
- Application #
- M022
- Marketing Start
- 03/25/2011
Recall History
No Recall HistoryFrequently Asked Questions
What is AQUAFRESH EXTREME CLEAN WHITENING ACTION used for?
AQUAFRESH EXTREME CLEAN WHITENING ACTION contains sodium fluoride. It is a paste taken dental. Consult your doctor for specific uses.
Is AQUAFRESH EXTREME CLEAN WHITENING ACTION a controlled substance?
AQUAFRESH EXTREME CLEAN WHITENING ACTION is not classified as a controlled substance by the DEA.
What is the generic name for AQUAFRESH EXTREME CLEAN WHITENING ACTION?
The generic name for AQUAFRESH EXTREME CLEAN WHITENING ACTION is sodium fluoride. There are 12 other brand versions of sodium fluoride.
What is the NDC code for AQUAFRESH EXTREME CLEAN WHITENING ACTION 1.13 mg/g?
The NDC (National Drug Code) for AQUAFRESH EXTREME CLEAN WHITENING ACTION 1.13 mg/g is 0135-0234, 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)