Home NDC 62032-539 Obagi Nu-Derm FX System Normal - Dry
Product NDC 62032-539
11-digit product format 620320539
Labeler code 62032
Product ID 62032-539_0ad34be9-6f0d-446b-8131-94f8e5f453b9
Type HUMAN OTC DRUG
Nonproprietary name Homosalate, Octisalate, and 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 Additional Listing Data#
Finished product Yes
Brand name base Obagi Nu-Derm FX System Normal - Dry
Brand name suffix Skin Transformation Complexion Brightening System
Listing expiration 2026-12-31 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 62032-539-07 Obagi Nu-Derm FX System Normal - Dry Skin Transformation Complexion Brightening System 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 62032-539 OBAGI NU-DERM FX SYSTEM NORMAL - DRY SKIN TRANSFORMATION COMPLEXION BRIGHTENING SYSTEM (HOMOSALATE, OCTISALATE, AND ZINC OXIDE) KIT [OBAGI COSMECEUTICALS LLC] 3 Current NDC, Legacy NDC, 1 package rows 20250406_512b20f0-60c8-47d4-a732-22fc999980d3.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 62032-539-07 62032053907 1 KIT in 1 CARTON (62032-539-07) * 57 g in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC * 48 g in 1 BOTTLE, PLASTIC * 85 g in 1 TUBE * 57 g in 1 BOTTLE, PLASTIC * 198 mL in 1 BOTTLE, PLASTIC * 198 mL in 1 BOTTLE, PLASTIC 1 kit 2019-12-02 0000-00-00 No No Current