UNIVERSAL ADVANCED WHITENING ANTI-CAVITY FLUORIDE .76 g/100g
Sodium Monofluorophosphate · PASTE · Universal Distribution Center LLC
UNIVERSAL ADVANCED WHITENING ANTI-CAVITY FLUORIDE is a paste containing sodium monofluorophosphate at .76 g/100g, taken dental. Manufactured by Universal Distribution Center LLC.
Key Facts
- Brand Name
- UNIVERSAL ADVANCED WHITENING ANTI-CAVITY FLUORIDE
- Generic Name
- Sodium Monofluorophosphate
- NDC Code (Product)
52000-112- Manufacturer
- Universal Distribution Center LLC
- Strength
- .76 g/100g
- Dosage Form
- PASTE
- Route
- DENTAL
- Marketing Status
- Application #
- M021
- Marketing Start
- 05/30/2020
Recall History
No Recall HistoryFrequently Asked Questions
What is UNIVERSAL ADVANCED WHITENING ANTI-CAVITY FLUORIDE used for?
UNIVERSAL ADVANCED WHITENING ANTI-CAVITY FLUORIDE contains Sodium Monofluorophosphate. It is a paste taken dental. Consult your doctor for specific uses.
Is UNIVERSAL ADVANCED WHITENING ANTI-CAVITY FLUORIDE a controlled substance?
UNIVERSAL ADVANCED WHITENING ANTI-CAVITY FLUORIDE is not classified as a controlled substance by the DEA.
What is the generic name for UNIVERSAL ADVANCED WHITENING ANTI-CAVITY FLUORIDE?
The generic name for UNIVERSAL ADVANCED WHITENING ANTI-CAVITY FLUORIDE is Sodium Monofluorophosphate. There are 12 other brand versions of Sodium Monofluorophosphate.
What is the NDC code for UNIVERSAL ADVANCED WHITENING ANTI-CAVITY FLUORIDE .76 g/100g?
The NDC (National Drug Code) for UNIVERSAL ADVANCED WHITENING ANTI-CAVITY FLUORIDE .76 g/100g is 52000-112, listed by Universal Distribution Center 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)