Home NDC 62032-529-06 nu-derm system normal-dry
Product NDC 62032-529
Requested package NDC 62032-529-06
11-digit product format 620320529
Labeler code 62032
Product ID 62032-529_ed79404d-956a-4f71-b348-3e89930fac3d
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Hydroquinone, Octisalate and Zinc Oxide
Dosage form KIT
Labeler OBAGI COSMECEUTICAL 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 · 4 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Code, Status table Captured / source date Code Status Snapshot Source SHA-256 2025-03-10 12:48 UTC · source 2025-03-10 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
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 nu-derm system normal-dry
Brand name suffix skin transformation
Listing expiration 2026-12-31 Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 197795 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 62032-100-36 nu-derm system normal-dry skin transformation 57 g in 1 BOTTLE, PLASTIC CREAM 57 g 40 mg in 1g 3 62032-101-36 nu-derm system normal-dry skin transformation 57 g in 1 BOTTLE, PLASTIC CREAM 57 g 40 mg in 1g 3 62032-141-10 nu-derm system normal-dry skin transformation 85 g in 1 TUBE LOTION 85 g 100 mg in 1g 3 62032-529-06 nu-derm system normal-dry skin transformation 1 in 1 CARTON KIT 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 62032-529 NU-DERM SYSTEM NORMAL-DRY SKIN TRANSFORMATION (HYDROQUINONE, OCTISALATE AND ZINC OXIDE) KIT [OBAGI COSMECEUTICAL LLC] 3 Current NDC, Legacy NDC, 4 package rows 20250316_7548658a-5371-4aed-baf8-e5dc54262223.zip
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.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 62032-529-06 62032052906 1 KIT in 1 CARTON (62032-529-06) * 57 g in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC (62032-100-36) * 48 g in 1 BOTTLE, PLASTIC * 85 g in 1 TUBE (62032-141-10) * 57 g in 1 BOTTLE, PLASTIC (62032-101-36) * 198 mL in 1 BOTTLE, PLASTIC * 198 mL in 1 BOTTLE, PLASTIC 1 kit 2019-12-02 0000-00-00 No No Current