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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| Benzalkonium Chloride | ANTIBACTERIAL HAND WIPES | Target Corporation | f6037707-c6bb-11a0-e053-2995a90acce8 | 2025-12-05 | Warnings | F5UM2KM3W7 |
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| CVS Health Maximum Strength | ANTACID AND ANTIGAS | CVS Pharmacy,Inc. | 0a13ac81-0c63-48c1-bbb0-f6e67f97b896 | 2025-12-04 | Warnings | 92RU3N3Y1O |
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| Sugargirl SPF 30 sunscreen illuminating stick sunlight | HOMOSALATE ,OCTOCRYLENE ,OCTISALATE , AVOBENZONE | Longway Technology(Guangzhou)Co.,Ltd. | 451b71a9-2240-853f-e063-6394a90ac8f4 | 2025-12-04 | Warnings | V06SV4M95S 4X49Y0596W |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.