NDC 62032-142 - Obagi-C Fx System Normal-Oily Skin Brightening System With Arbutin
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 62032-142
- Package NDCs from labels
- 62032-142-11
- Manufacturer
- Obagi Cosmeceuticals LLC | Universal Packaging Systems, Inc. DBA: PakLab | Swiss American CDMO, LLC | Bay Cities Container Corporation
- Effective date
- 2019-10-29
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| OBAGI-C ® FX SYSTEM NORMAL-OILY SKIN BRIGHTENING SYSTEM WITH ARBUTIN | Obagi Cosmeceuticals LLC | Universal Packaging Systems, Inc. DBA: PakLab | Swiss American CDMO, LLC | Bay Cities Container Corporation | 2019-10-29 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 62032-142-11 | Obagi-C Fx System Normal-Oily Skin Brightening System With Arbutin | 85 g in 1 TUBE | LOTION | 85 g | 50 mg in 1g | 1 |
DailyMed Dashboard NDC Coverage#
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.