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LIGHTENER

FULL PRESCRIBING INFORMATION

DURING AND AFTER TREATMENT EXPOSURE TO SUN MUST BE AVOIDED BY SUNSCREEN USAGE OR PROTECTIVE CLOTHING.

IF NO BLEACHING IS NOTICED AFTER 3 MONTHS, STOP TREATMENT.

DO NOT USE ON CHILDREN UNDER 12 YEARS OF AGE.

DO NOT APPLY TO INFLAMED OR BROKEN AREA.

HYDROQUINONE CREAM

Product Information
Product Type	Human otc drug label	Item Code (Source)	NDC:66538-201
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Hydroquinone HYDROQUINONE		1.9 g

Inactive Ingredients
Ingredient Name	Strength
water
SAFFLOWER OIL
EGG PHOSPHOLIPIDS
ISOPROPYL PALMITATE
DIETHYLENE GLYCOL MONOETHYL ETHER
GLYCERYL MONOSTEARATE
PEG-100 STEARATE
XANTHAN GUM
LACTIC ACID
TETRAHEXYLDECYL ASCORBATE
DMDM HYDANTOIN
IODOPROPYNYL BUTYLCARBAMATE
METHYLISOTHIAZOLINONE
SODIUM BICARBONATE
BUTYLENE GLYCOL
SODIUM METABISULFITE
GLYCYRRHIZA GLABRA
METHYLPARABEN
PROPYLPARABEN
BUTYLPARABEN

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC:66538-201-12	50 in 1 JAR

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
partA	part358A	2011-11-30

PLEASE, BE CAREFUL!

Be sure to consult your doctor before taking any medication!