NDC 62032-141 - nu-derm system normal-dry skin transformation
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
- 62032-141
- Package NDCs from labels
- 62032-141-10
- Manufacturer
- OBAGI COSMECEUTICAL LLC | PURETEK CORPORATION | Swiss-American CDMO, LLC | G. S. Cosmeceutical USA, Inc.
- Effective date
- 2025-03-14
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| OBAGI NU-DERM ® SYSTEM | OBAGI COSMECEUTICAL LLC | PURETEK CORPORATION | Swiss-American CDMO, LLC | G. S. Cosmeceutical USA, Inc. | 2025-03-14 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 62032-141-10 | nu-derm system normal-dry skin transformation | 85 g in 1 TUBE | LOTION | 85 g | 100 mg in 1g | 3 |
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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| Sodium Chloride | SODIUM CHLORIDE | Fresenius Medical Care de Mexico, S.A. de C.V. | 9a1220fb-6853-45ae-838c-10d8596e1af7 | 2026-07-27 | Warnings, Adverse reactions | 451W47IQ8X |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.