BRIGHTEN LIGHTENING- hydroquinone gel 
CEN BEAUTY LLC

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.

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ACTIVE INGREDIENT

ZINC OXIDE 15%

OCTINOXATE 6%

PURPOSE

SUNSCREEN

USES

WARNINGS

FOR EXTERNAL USE ONLY

DO NOT USE

WHEN USING THIS PRODUCT

STOP USE AND ASK A DOCTOR IF RASH OCCURS.

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

ASK A DOCTOR BEFORE USE

DIRECTIONS

Other Information

INGREDIENTS

aqua (water), cyclopentasiloxane, PEG-10 dimethicone, dimethicone, butylene glycol, cyclohexasiloxane, glycerin, carollina officinalis extract, algae extract, avena sativa (oat) kernel extract, angelica sinensis extract, 10-hydroxydecanoic acid, sebacic acid, 1,10-decanediol acid, betaine, dimethicone/vinyl dimethicone crosspolymer, lauryl PEG-9 polydimethylsiloxyethyl dimethicone, lecithin, dimethicone/PEG-10/15 crosspolymer, triethoxycaprylylsilane, decamethylcyclopentasiloxane, trifluoromethyl C1-C4 alkyl dimethicone, quaternium-90, bentonite, butylene glycol, sodium chloride, sodium citrate, ethylhexylglycerin, propylene carbonate, propylene glycol, potassium sorbate, methylisothiazolinone, iodopropynyl butylcarbamate, phenoxyethanol

BB_Lightening Gel-HQ_1oz_Tubes_ARTWORK_FRBB_Lightening Gel-HQ CX621

BRIGHTEN  LIGHTENING
hydroquinone gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54272-301
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE) HYDROQUINONE2 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ASCORBIC ACID (UNII: PQ6CK8PD0R)  
ALLANTOIN (UNII: 344S277G0Z)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
GLYCERIN (UNII: PDC6A3C0OX)  
OAT (UNII: Z6J799EAJK)  
ANGELICA SINENSIS WHOLE (UNII: 697D19QDBN)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
10-HYDROXYDECANOIC ACID (UNII: NP03XO416B)  
1,10-DECANEDIOL (UNII: 5I577UDK52)  
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
LACTIC ACID (UNII: 33X04XA5AT)  
GLYCERETH-7 TRIMETHYL ETHER (UNII: XMC7402M60)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
SODIUM METABISULFITE (UNII: 4VON5FNS3C)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
XANTHAN GUM (UNII: TTV12P4NEE)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:54272-301-1130 mL in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart358A02/21/2013
Labeler - CEN BEAUTY LLC (078664118)
Registrant - CEN BEAUTY LLC (078664118)

Revised: 3/2013
Document Id: 2d9bf516-a130-4aaf-8efb-600250a7236d
Set id: c4f30486-d2ae-403c-9113-3f2a5b1476d5
Version: 1
Effective Time: 20130305
 
CEN BEAUTY LLC