Obagi Nu-Derm Fx System Normal-Dry Skin Transformation Kit
- Product NDC
- 62032-903
- 11-digit product format
- 620320903
- Labeler code
- 62032
- Product ID
- 62032-903_cb284faa-845f-4ead-b322-1a7a212a1404
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Homosalate, Octisalate, Zinc Oxide
- Dosage form
- KIT
- Labeler
- Obagi Cosmeceuticals LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2019-12-02
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Obagi Nu-Derm Fx System Normal-Dry Skin Transformation Kit
- Brand name suffix
- Complexion Brightening System
- Listing expiration
- 2026-12-31
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 62032-140-09 | Obagi Nu-Derm Fx System Normal-Dry Skin Transformation KitComplexion Brightening System | 85 g in 1 TUBE | LOTION | 85 g | 50 mg in 1g | 3 |
| 62032-140-09 | Obagi Nu-Derm Fx System Normal-Dry Skin Transformation KitComplexion Brightening System | 1 in 1 CARTON | LOTION | | 50 mg in 1g | 3 |
| 62032-903-32 | Obagi Nu-Derm Fx System Normal-Dry Skin Transformation KitComplexion Brightening System | 1 in 1 CARTON | KIT | 1 | | 3 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 62032-140-09 | 62032014009 | 85 g in 1 TUBE | 85 g | Historical |
| 62032-903-32 | 62032090332 | 1 in 1 CARTON | | Historical |