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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| MG DermaGel 62 LV | ETHYL ALCOHOL | Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc. | 437a508d-31ba-49b4-b821-4bf57b596e33 | 2025-12-23 | Warnings | 3K9958V90M |
| Antibacterial Liquid Hand | BENZALKONIUM CHLORIDE | Morgan Gallacher Inc. DBA Custom Chemical Formulators Inc. | ea0a5970-e95f-4090-bbe3-7df9e04393b5 | 2025-12-23 | Warnings | F5UM2KM3W7 |
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| MG DermaSan | N/A | Morgan Gallacher Inc. | d4c0de39-8570-4a05-a5e3-3752545ed95f | 2025-12-23 | Warnings | F5UM2KM3W7 |
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| Foaming Antibacterial Handsoap | BENZALKONIUM CHLORIDE | Chemcor Chemical Corporation | eed9b007-0dc1-4954-891f-a7a042e763aa | 2025-12-22 | Warnings | F5UM2KM3W7 |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.