FDA.reportPublic FDA data

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 table
LabelManufacturerEffective dateType
OBAGI NU-DERM ® SYSTEMOBAGI COSMECEUTICAL LLC | PURETEK CORPORATION | Swiss-American CDMO, LLC | G. S. Cosmeceutical USA, Inc.2025-03-14HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62032-141-10nu-derm system normal-dry skin transformation85 g in 1 TUBELOTION85 g100 mg in 1g3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62032-141NU-DERM SYSTEM NORMAL-DRY SKIN TRANSFORMATION (HYDROQUINONE, OCTISALATE AND ZINC OXIDE) KIT [OBAGI COSMECEUTICAL LLC]3Unmatched20250316_7548658a-5371-4aed-baf8-e5dc54262223.zip