NDC Code(s) : 69269-105-36
Packager : YS PLUS CORPORATION

Category : HUMAN PRESCRIPTION DRUG LABEL

DEA Schedule : none

Marketing Status : New Drug Application

INGREDIENTS AND APPEARANCE

Obagi - C HYDROQUINONE LIQUID
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:69269-105
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
HYDROQUINONE(UNII: XV74C1N1AE)
(HYDROQUINONE - UNII:XV74C1N1AE) 		HYDROQUINONE40 mg in 1 g
Inactive Ingredients
Ingredient Name Strength
WATER(UNII: 059QF0KO0R)
GLYCERIN(UNII: PDC6A3C0OX)
CETYL ALCOHOL(UNII: 936JST6JCN)
PPG-2 MYRISTYL ETHER PROPIONATE(UNII: 88R97D8U8A)
SODIUM LAURYL SULFATE(UNII: 368GB5141J)
TROLAMINE SALICYLATE(UNII: H8O4040BHD)
LACTIC ACID(UNII: 33X04XA5AT)
PHENYL TRIMETHICONE(UNII: DR0K5NOJ4R)
.ALPHA.-TOCOPHEROL ACETATE(UNII: 9E8X80D2L0)
SODIUM DITHIONATE(UNII: RPF7Z41GAW)
ASCORBIC ACID(UNII: PQ6CK8PD0R)
METHYLPARABEN(UNII: A2I8C7HI9T)
EDETATE DISODIUM(UNII: 7FLD91C86K)
PROPYLPARABEN(UNII: Z8IX2SC1OH)
BUTYLATED HYDROXYTOLUENE(UNII: 1P9D0Z171K)
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1NDC:69269-105-3657 g in 1 BOTTLE, PLASTIC
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 10/01/2014

PRINCIPAL DISPLAY PANEL

copy of label