"62032-509-01" National Drug Code (NDC)

NDC Code	62032-509-01
Package Description	1 KIT in 1 CARTON (62032-509-01) * 90 mL in 1 BOTTLE, PLASTIC (62032-119-90) * 200 mL in 1 BOTTLE, PLASTIC * 200 mL in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC * 57 g in 1 BOTTLE, PLASTIC (62032-117-36) * 57 g in 1 BOTTLE, PLASTIC (62032-115-36)
Product NDC	62032-509
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Condition And Enhance System
Proprietary Name Suffix	Full-size Non-surgical
Non-Proprietary Name	Hydroquinone, Octinoxate And Zinc Oxide
Dosage Form	KIT
Start Marketing Date	20070820
Marketing Category Name	UNAPPROVED DRUG OTHER
Manufacturer	OMP, INC.