Obagi-C Fx System Normal-Oily Skin Brightening System with Arbutin
- Product NDC
- 62032-917
- 11-digit product format
- 620320917
- Labeler code
- 62032
- Product ID
- 62032-917_a27a6106-f8cb-47e4-8e71-1f7dceb77d3d
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Obagi-C Fx System Normal-Oily Skin Brightening System with Arbutin
- Listing expiration
- 2027-12-31
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 62032-140-09 | Obagi-C Fx System Normal-Oily Skin Brightening System with Arbutin | 1 in 1 CARTON | LOTION | | 100 mg in 1g | 3 |
| 62032-140-09 | Obagi-C Fx System Normal-Oily Skin Brightening System with Arbutin | 85 g in 1 TUBE | LOTION | 85 g | 100 mg in 1g | 3 |
| 62032-917-01 | Obagi-C Fx System Normal-Oily Skin Brightening System with Arbutin | 1 in 1 CARTON | KIT | 1 | | 3 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 62032-140-09 | 62032014009 | 1 in 1 CARTON | Historical |
| 62032-917-01 | 62032091701 | 1 in 1 CARTON | Historical |