Pill Identifier App

LIGHTENER

Dosage form: cream
Ingredients: HYDROQUINONE 1.9g in 100g
Labeler: CRC (Cosmoceutical Research Center)
NDC Code: 66538-201

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.

LIGHTENER

ACTIVE INGREDIENTS:
HYDROQUINONE 1.9%

PURPOSE:
SKIN LIGHTENING

INDICATION:
FOR GRADUAL FADING OF FRECKLES AND AGE SPOTS.
HELPS SKIN DISCOLORATION THAT MAY RESULT FROM PREGNANCY OR USE OF ORAL CONTRACEPTIVE.

WARNING: FOR EXTERNAL USE ONLY.

KEEP OUT OF REACH OF CHILDREN.

DIRECTIONS: A THIN LAYER SHOULD BE APPLIED TO THE ENTIRE FACE TWICE DAILY OR AS DIRECTED.

INACTIVE INGREDIENTS: PURIFIED WATER, SAFFLOWER OIL, PHOSPHOLIPIDS, ISOPROPYL PALMITATE, ETHOXYDIGLYCOL, GLYCERYL STEARATE, PEG-100 STEARATE, XANTHAN GUM, LACTIC ACID, TETRAHEXYLDECYL ASCORBATE, DMDM HYDANTOIN, IODOPROPYNYL BUTYLCARBAMATE, METHYLISOTHIAZOLINONE, SODIUM BICARBONATE, BUTYLENE GLYCOL, SODIUM METABISULFITE, LICORICE EXTRACT, METHYLPARABEN, PROPYLPARABEN, BUTYLPARABEN.

CRC
LIGHTENER
HYDROQUINONE 1.9%
WITH LICORICE AND VITAMIN C
1.75 OZ. (50G)

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.

LIGHTENER 
hydroquinone cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66538-201
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROQUINONE (HYDROQUINONE) HYDROQUINONE1.9 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
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 CodePackage Description
1NDC:66538-201-1250 g in 1 JAR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart358A11/30/2011
Labeler - CRC (Cosmoceutical Research Center) (160019006)
Registrant - CRC (Cosmoceutical Research Center) (160019006)

Revised: 11/2011
 
CRC (Cosmoceutical Research Center)

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.

Hide
(web2)