Home NDC 62032-903 Obagi Nu-Derm Fx System Normal-Dry Skin Transformation Kit
Product NDC 62032-903
11-digit product format 620320903
Labeler code 62032
Product ID 62032-903_cb284faa-845f-4ead-b322-1a7a212a1404
Type HUMAN OTC DRUG
Nonproprietary name Homosalate, Octisalate, Zinc Oxide
Dosage form KIT
Labeler Obagi Cosmeceuticals LLC
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2019-12-02
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 1 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 62032-903 62032-903-32 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Obagi Nu-Derm Fx System Normal-Dry Skin Transformation Kit
Brand name suffix Complexion Brightening System
Listing expiration 2026-12-31 Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 62032-140-09 Obagi Nu-Derm Fx System Normal-Dry Skin Transformation KitComplexion Brightening System 85 g in 1 TUBE LOTION 85 g 50 mg in 1g 3 62032-140-09 Obagi Nu-Derm Fx System Normal-Dry Skin Transformation KitComplexion Brightening System 1 in 1 CARTON LOTION 50 mg in 1g 3 62032-903-32 Obagi Nu-Derm Fx System Normal-Dry Skin Transformation KitComplexion Brightening System 1 in 1 CARTON KIT 1 3
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.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Status 62032-140-09 62032014009 85 g in 1 TUBE 85 g Historical 62032-903-32 62032090332 1 in 1 CARTON Historical