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.
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| GoodSense SPF 30 Sunscreen | AVOBENZONE 3%, HOMOSALATE 15%, OCTISALATE 5%, OCTOCRYLENE 6% | Geiss, Destin, & Dunn, Inc. | c85c5d2b-35f6-2fd5-e053-2995a90a4a53 | 2025-11-09 | Warnings | V06SV4M95S 4X49Y0596W |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.