LIGHT THE WAY- hydroquinone lotion

LIGHT THE WAY by

Drug Labeling and Warnings

LIGHT THE WAY by is a Otc medication manufactured, distributed, or labeled by mybody. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ACTIVE INGREDIENT         HYDROQUINONE 2%

PURPOSE

PURPOSE         SKIN LIGHTENING

INDICATIONS & USAGE

USE  GRADUALLY AND EFFECTIVELY LIGHTENS DARK AREAS IN THE SKIN

WARNINGS

WARNINGS

FOR EXTERNAL USE ONLY

DO NOT USE

DO NOT USE

• ON INFLAMED OR BROKEN SKIN.
• FOR THE PREVENTION OF SUNBURN.
• AS A SUNSCREEN.
  

ASK DOCTOR

ASK A DOCTOR OR PHARMACIST BEFORE USE IF

• PREGNANT OR LACTATING.
• IN COMBINATION WITH PRODUCTS CONTAINING RESORCINOL, PHENOL, OR SALICYLIC ACID.
• BY CHILDREN UNDER THE AGE OF 12.
  

STOP USE

STOP USE AND ASK A DOCTOR

• IF AREAS DARKEN OR BLUE-BLACK DARKENING OCCURS.
• MILD IRRITATION MAY OCCUR. IF IRRITATION BECOMES SEVERE, STOP USE AND CONSULT A DOCTOR.
  

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF CHILDREN * IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

DOSAGE & ADMINISTRATION

DIRECTIONS

• ADULTS ONLY
• PM: APPLY SIDE 1 HYDROQUINONE TO CLEAN SKIN. ALLOW TO DRY. NEXT APPLY SIDE 2 WITH RETINOL. ALLOW TO DRY. DAILY USE OF SUNSCREEN IS RECOMMENDED.
• FOR BEST RESULTS: APPLY MYBODY'S PROTECT AND SERVE SUN SHIELD SPF 30 (AM ONLY) WHEN USING LIGHT THE WAY.
• FOR SENSITIVE SKIN, TEST OVERNIGHT ON SMALL AREA (INSIDE ELBOW).
• IF NO IMPROVEMENT IS SEEN AFTER 3 MONTHS, DISCONTINUE USE. ON VERY DARK SKIN, LIGHTENING EFFECT MAY NOT BE NOTICEABLE.
• TO PREVENT DARKENING FROM REOCCURRING, USE A SUNSCREEN OR WEAR PROTECTIVE CLOTHING TO COVER TREATED SKIN DURING AND AFTER PRODUCT USE.
  

OTHER SAFETY INFORMATION

OTHER INFORMATION

* AVOID STORAGE AT EXTREME TEMPERATURES (BELOW 40°F AND ABOVE 100°F).

INACTIVE INGREDIENT

INACTIVE INGREDIENTS CHAMBER A: WATER,  HEXYL LAURATE, GLYCERYL STEARATE SE, CETYL ALCOHOL, CAPRYLIC/CAPRIC TRIGLYCERIDE, STEARIC ACID, BUTYROSPERMUM PARKII (SHEA BUTTER), GLYCERIN, CETETH-2, BEHENYL ALCOHOL, HYDROXYPROPYL STARCH PHOSPHATE, XANTHAN GUM, POTASSIUM HYDROXIDE, SODIUM SULFITE, FRAGRANCE, CAPRYLYL GLYCOL, PHENOXYETHANOL, CITRIC ACID, SODIUM METABISULFITE.

QUESTIONS

QUESTIONS OR COMMENTS?

CALL 877.423.1314 * WWW.LOVEMYBODY.COM

PRINCIPAL DISPLAY PANEL

MYBODY

LIGHT THE WAY

BOOSTER PACK: HYPERPIGMENTATION

MYBOOSTER * STEP 2

WHEN USING

WHEN USING THIS PRODUCT

• AVOID CONTACT WITH EYES.
• LIMIT SUN EXPOSURE.
  

INGREDIENTS AND APPEARANCE

LIGHT THE WAY 
hydroquinone lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49520-201
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE)	HYDROQUINONE	2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
HEXYL LAURATE (UNII: 4CG9F9W01Q)
GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
CETYL ALCOHOL (UNII: 936JST6JCN)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
STEARIC ACID (UNII: 4ELV7Z65AP)
SHEA BUTTER (UNII: K49155WL9Y)
GLYCERIN (UNII: PDC6A3C0OX)
CETETH-2 (UNII: 7H8VAM7778)
DOCOSANOL (UNII: 9G1OE216XY)
HYDROXYPROPYL CORN STARCH (5% SUBSTITUTION BY WEIGHT) (UNII: 9M44R3409A)
XANTHAN GUM (UNII: TTV12P4NEE)
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
SODIUM SULFITE (UNII: VTK01UQK3G)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM METABISULFITE (UNII: 4VON5FNS3C)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49520-201-51	1 in 1 BOX
1	NDC: 49520-201-11	15 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part358A	04/24/2012

Labeler - mybody (004460532)

Registrant - mybody (004460532)