Home NDC 62032-532 NU-DERM system NORMAL-DRY
Product NDC 62032-532
11-digit product format 620320532
Labeler code 62032
Product ID 62032-532_11f43e07-efe3-4959-b6fb-91ae51485f5f
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Hydroquinone, Homosalate, 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 Additional Listing Data#
Finished product Yes
Brand name base NU-DERM system NORMAL-DRY
Brand name suffix SKIN TRANSFORMATION TRIAL
Listing expiration 2026-12-31 Harmonized Identifiers# Field, Values table Field Values Rxcui 197795
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 62032-532-07 NU-DERM system NORMAL-DRY SKIN TRANSFORMATION TRIAL 1 in 1 CARTON KIT 1 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 62032-532 NU-DERM SYSTEM NORMAL-DRY SKIN TRANSFORMATION TRIAL (HYDROQUINONE, HOMOSALATE, OCTISALATE, AND ZINC OXIDE) KIT [OBAGI COSMECEUTICAL LLC] 5 Current NDC, Legacy NDC, 1 package rows 20250316_e2fd24f9-f517-4b21-812c-ad4d56c27bc4.zip
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 62032-532-07 62032053207 1 KIT in 1 CARTON (62032-532-07) * 59 mL in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC * 28 g in 1 BOTTLE, PLASTIC * 85 g in 1 TUBE * 59 mL in 1 BOTTLE, PLASTIC * 28 g in 1 BOTTLE, PLASTIC 1 kit 2019-12-02 0000-00-00 No No Current