INDICATIONS & USAGE SECTION.

USES:FOR THE GRADUAL FADING OF DARK AREAS OF THE SKIN.

DOSAGE & ADMINISTRATION SECTION.

DIRECTIONS:ADULTS: APPLY SMALL AMOUNT AS THIN LAYER ON THE AFFECTED AREA TWICE DAILY, OR USE AS DIRECTED BY DOCTOR. IF NO IMPROVEMENT IS SEEN AFTER MONTHS OF TREATMENT, USE OF THIS PRODUCT SHOULD BE DISCONTINUED. LIGHTENING EFFECT OF THIS PRODUCT MAY NOT BE NOTICEABLE WHEN USED ON VERY DARK SKIN. CHILDREN UNDER 12 YEARS OF AGE: DO NOT USE UNLESS DIRECTED BY DOCTOR.

INACTIVE INGREDIENT SECTION.

INACTIVE INGREDIENTS:ALPHA ARBUTIN, C13-14 ISOPARAFFIN, CETYL ALCOHOL, ETHYLHEXYLGLYCERIN, ETHYLHEXYL STEARATE, GLYCERIN, GLYCERYL STEARATE, GLYCOLIC ACID, ISOPROPYL MYRISTATE, LAURETH-7, NIACINAMIDE, PANTOTHENIC ACID, PEG-100 STEARATE, PHENOXYETHANOL, PHENYLETHYL RESORCINOL, POLYACRYLAMIDE, PYRIDOXINE HCL, SODIUM HYDROXIDE, SODIUM METABISULFITE, TETRAHEXYLDECYL ASCORBATE, WATER (AQUA), XANTHAN GUM.

OTHER SAFETY INFORMATION.

THIS PRODUCT IS NOT INTENDED FOR USE IN THE PREVENTION OF SUNBURN AND CONTAINS AN ALPHA HYDROXY ACID (AHA) THAT MAY INCREASE YOUR SKINS SENSITIVITY TO THE SUN AND PARTICULARLY THE POSSIBILITY OF SUNBURN. SUN EXPOSURE SHOULD BE LIMITED BY USING SUNSCREEN AGENT OR PROTECTIVE CLOTHING TO COVER BLEACHED SKIN AFTER TREATMENT IS COMPLETED TO PREVENT DARKENING FROM REOCCURING.

OTC - ACTIVE INGREDIENT SECTION.

ACTIVE INGREDIENTS:HYDROQUINONE USP 2%.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION.

KEEP OUT OF REACH OF CHILDREN.

OTC - PURPOSE SECTION.

PURPOSE:SKIN LIGHTENING.

OTC - QUESTIONS SECTION.

QUESTIONS 1-323-733-7033.

OTC - STOP USE SECTION.

IF IRRITATION BECOMES SEVERE, STOP USE AND CONSULT DOCTOR.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL.

Lady-Lightening42952-203-12.

WARNINGS SECTION.

WARNINGS:AVOID CONTACT WITH EYES. SOME USERS MAY EXPERIENCE MILD SKIN IRRITATION.