Obagi Nu-Derm Fx System Normal-Dry Skin Transformation Complexion Brightening System
Titanium Dioxide, Zinc Oxide · KIT · Obagi Cosmeceuticals LLC
Obagi Nu-Derm Fx System Normal-Dry Skin Transformation Complexion Brightening System is a kit containing titanium dioxide, zinc oxide. Manufactured by Obagi Cosmeceuticals LLC.
Key Facts
- Brand Name
- Obagi Nu-Derm Fx System Normal-Dry Skin Transformation Complexion Brightening System
- Generic Name
- Titanium Dioxide, Zinc Oxide
- NDC Code (Product)
62032-924- Manufacturer
- Obagi Cosmeceuticals LLC
- Dosage Form
- KIT
- Marketing Status
- Application #
- M020
- Marketing Start
- 06/25/2025
Recall History
No Recall HistoryFrequently Asked Questions
What is Obagi Nu-Derm Fx System Normal-Dry Skin Transformation Complexion Brightening System used for?
Obagi Nu-Derm Fx System Normal-Dry Skin Transformation Complexion Brightening System contains Titanium Dioxide, Zinc Oxide. It is a kit taken as directed. Consult your doctor for specific uses.
Is Obagi Nu-Derm Fx System Normal-Dry Skin Transformation Complexion Brightening System a controlled substance?
Obagi Nu-Derm Fx System Normal-Dry Skin Transformation Complexion Brightening System is not classified as a controlled substance by the DEA.
What is the generic name for Obagi Nu-Derm Fx System Normal-Dry Skin Transformation Complexion Brightening System?
The generic name for Obagi Nu-Derm Fx System Normal-Dry Skin Transformation Complexion Brightening System is Titanium Dioxide, Zinc Oxide. There are 12 other brand versions of Titanium Dioxide, Zinc Oxide.
What is the NDC code for Obagi Nu-Derm Fx System Normal-Dry Skin Transformation Complexion Brightening System ?
The NDC (National Drug Code) for Obagi Nu-Derm Fx System Normal-Dry Skin Transformation Complexion Brightening System is 62032-924, listed by Obagi Cosmeceuticals 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)