Home NDC 62032-914 Obagi Nu-Derm System Normal-Oily Skin Transformation Trial
Product NDC 62032-914
11-digit product format 620320914
Labeler code 62032
Product ID 62032-914_bc389b46-a94e-4cc3-baec-73044c6a387f
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Hydroquinone, 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 Additional Listing Data#
Finished product Yes
Brand name base Obagi Nu-Derm System Normal-Oily Skin Transformation Trial
Listing expiration 2026-12-31 Harmonized Identifiers# Field, Values table Field Values Rxcui 197795
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 62032-101-36 Obagi Nu-Derm System Normal-Oily Skin Transformation Trial 57 g in 1 BOTTLE, PLASTIC CREAM 57 g 40 mg in 1g 3 62032-140-05 Obagi Nu-Derm System Normal-Oily Skin Transformation Trial 28 g in 1 TUBE LOTION 28 g 100 mg in 1g 3 62032-914-01 Obagi Nu-Derm System Normal-Oily Skin Transformation Trial 1 in 1 KIT KIT 1 3
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 62032-101-36 62032010136 57 g in 1 BOTTLE, PLASTIC 57 g Historical 62032-140-05 62032014005 28 g in 1 TUBE 28 g Historical 62032-914-01 62032091401 1 KIT in 1 KIT (62032-914-01) * 57 g in 1 BOTTLE, PLASTIC (62032-101-36) * 28 g in 1 BOTTLE, PLASTIC * 28 g in 1 BOTTLE, PLASTIC * 28 g in 1 TUBE (62032-140-05) * 59 mL in 1 BOTTLE, PLASTIC * 59 mL in 1 BOTTLE, PLASTIC 1 kit 2021-06-25 No No Current