Home NDC 62032-905 Obagi Skintrinsiq Brightening Protocol
Product NDC 62032-905
11-digit product format 620320905
Labeler code 62032
Product ID 62032-905_2b80c4d4-9623-46b8-8993-8105b0a16f2a
Type HUMAN OTC DRUG
Nonproprietary name HOMOSALATE, OCTISALATE, AND ZINC OXIDE
Dosage form KIT
Labeler Obagi Cosmeceuticals LLC
Application M020
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-08-01
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Obagi Skintrinsiq Brightening Protocol
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 62032-140-09 Obagi Skintrinsiq Brightening Protocol 1 in 1 CARTON LOTION 100 mg in 1g 3 62032-140-09 Obagi Skintrinsiq Brightening Protocol 85 g in 1 TUBE LOTION 85 g 50 mg in 1g 3 62032-905-05 Obagi Skintrinsiq Brightening Protocol 1 in 1 BOX KIT 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 62032-905 OBAGI SKINTRINSIQ BRIGHTENING PROTOCOL (HOMOSALATE, OCTISALATE, AND ZINC OXIDE) KIT [OBAGI COSMECEUTICALS LLC] 3 Current NDC, Legacy NDC, 3 package rows 20250406_2f75ebf7-d6b6-45c6-ad5b-61739d260ff7.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 62032-140-09 62032014009 1 in 1 CARTON Historical 62032-905-05 62032090505 1 KIT in 1 BOX (62032-905-05) * 57 g in 1 BOTTLE, PLASTIC * 1 BOTTLE, PUMP in 1 CARTON / 48 g in 1 BOTTLE, PUMP * 1 TUBE in 1 CARTON (62032-140-09) / 85 g in 1 TUBE * 59 mL in 1 BOTTLE, PLASTIC * 60 mL in 1 BOTTLE, PLASTIC 1 kit 2021-08-01 0000-00-00 No No Current