Home NDC 62032-131 GENTLE REJUVENATION ULTRA LIGHT REPAIR SPF 30
Product NDC 62032-131
11-digit product format 620320131
Labeler code 62032
Product ID 62032-131_13520a24-3b31-4653-9cd1-5cb1ef1c742d
Type HUMAN OTC DRUG
Nonproprietary name HOMOSALATE, OCTINOXATE, OCTOCRYLENE, and ZINC OXIDE
Dosage form CREAM
Route TOPICAL
Labeler Obagi Medical Products, Inc., a division of Valeant Pharmaceuticals North America LLC.
Application part352
Marketing category OTC MONOGRAPH FINAL
Marketing start 2013-10-15
Marketing end 0000-00-00
Substance HOMOSALATE; OCTINOXATE; OCTOCRYLENE; ZINC OXIDE
Active strength 120 mg/g; mg/g; mg/g; mg/g
NDC exclude flag E
Listing certified through 2017-12-31
Current FDA listing Historical FDA.report record FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 62032-131-70 GENTLE REJUVENATION ULTRA LIGHT REPAIR SPF 30SUNSCREEN 50 g in 1 TUBE CREAM 50 2 62032-131-70 GENTLE REJUVENATION ULTRA LIGHT REPAIR SPF 30SUNSCREEN 1 in 1 CARTON CREAM 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 62032-131 GENTLE REJUVENATION ULTRA LIGHT REPAIR SPF 30 SUNSCREEN (HOMOSALATE, OCTINOXATE, OCTOCRYLENE, AND ZINC OXIDE) CREAM [OBAGI MEDICAL PRODUCTS, INC., A DIVISION OF VALEANT PHARMACEUTICALS NORTH AMERICA LLC.] 2 Legacy NDC, 2 package rows 20150619_5222ba81-bb97-4f0a-a465-f61c0b1d28a4.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Status 62032-131-70 62032013170 50 g in 1 TUBE 50 g Historical