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LIGHT THE WAY

Medically reviewed on May 2, 2018

Dosage form: lotion
Ingredients: HYDROQUINONE 2g in 100mL
Labeler: mybody
NDC Code: 49520-201

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

LIGHT THE WAY

ACTIVE INGREDIENT         HYDROQUINONE 2%

PURPOSE         SKIN LIGHTENING

USE  GRADUALLY AND EFFECTIVELY LIGHTENS DARK AREAS IN THE SKIN

WARNINGS

FOR EXTERNAL USE ONLY

DO NOT USE

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

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 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 * IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

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 INFORMATION

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

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 OR COMMENTS?

CALL 877.423.1314 * WWW.LOVEMYBODY.COM

MYBODY

LIGHT THE WAY

BOOSTER PACK: HYPERPIGMENTATION

MYBOOSTER * STEP 2




WHEN USING THIS PRODUCT

  • AVOID CONTACT WITH EYES.
  • LIMIT SUN EXPOSURE.
LIGHT THE WAY 
hydroquinone lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49520-201
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROQUINONE (HYDROQUINONE) HYDROQUINONE2 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
HEXYL LAURATE 
GLYCERYL STEARATE SE 
CETYL ALCOHOL 
MEDIUM-CHAIN TRIGLYCERIDES 
STEARIC ACID 
SHEA BUTTER 
GLYCERIN 
CETETH-2 
DOCOSANOL 
HYDROXYPROPYL CORN STARCH (5% SUBSTITUTION BY WEIGHT) 
XANTHAN GUM 
POTASSIUM HYDROXIDE 
SODIUM SULFITE 
CAPRYLYL GLYCOL 
PHENOXYETHANOL 
CITRIC ACID MONOHYDRATE 
SODIUM METABISULFITE 
Packaging
#Item CodePackage Description
1NDC:49520-201-511 BOTTLE (BOTTLE) in 1 BOX
1NDC:49520-201-1115 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart358A04/24/2012
Labeler - mybody (004460532)
Registrant - mybody (004460532)

 
mybody

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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