"63742-025-01" National Drug Code (NDC)

NDC Code	63742-025-01
Package Description	44 g in 1 TUBE (63742-025-01)
Product NDC	63742-025
Product Type Name	HUMAN OTC DRUG
Proprietary Name	Dr. Lightening Ultra-potent Facial
Non-Proprietary Name	Hydroquinone
Dosage Form	CREAM
Usage	TOPICAL
Start Marketing Date	20190215
Marketing Category Name	OTC MONOGRAPH NOT FINAL
Application Number	part358A
Manufacturer	Clinical Resolution Laboratory, Inc.
Substance Name	HYDROQUINONE
Strength	20
Strength Unit	mg/g
Pharmacy Classes	Depigmenting Activity [PE], Melanin Synthesis Inhibitor [EPC], Melanin Synthesis Inhibitors [MoA]