DR. THROWERS SKIN LIGHTENING MOISTURIZING- hydroquinone lotion 
DR. THROWER'S SKINCARE, INC.

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

HYDROQUINONE 2%

PURPOSE

SKIN LIGHTENING

USES:

FOR THE GRADUAL FADING OF DARK AREAS IN THE SKIN SUCH AS FRECKLES, AGE AND LIVER SPOTS.

WARNINGS

FOR EXTERNAL USE ONLY.

WHEN USING THIS PRODUCT

DO NOT USE

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

DIRECTIONS

APPLY A SMALL AMOUNT AS A THIN LAYER ON THE AFFECTED AREA TWICE DAILY, OR USE AS DIRECTED BY A DOCTOR. IF NO IMPROVEMENT IS SEEN AFTER 3 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 A DOCTOR.

INACTIVE INGREDIENTS:

WATER, PROPYLENE GLYCOL, CETYL ALCOHOL, MINERAL OIL, GLYCERYL STEARATE, CETEARYL ALCOHOL, CETEARETH-20, POTATO STARCH MODIFIED, DIMETHICONE, FRAGRANCE, PHENOXYETHANOL, TRIMETHYLPROPANEDIOL/ADIPIC ACID COPOLYMER, LANOLIN, SODIUM METABISULFITE, METHYLPARABEN, CITRUS GRANDIS (GRAPEFRUIT) PEEL OIL, TETRASODIUM EDTA, PHOSPHOLIPIDS, TOCOPHERYL ACETATE, RETINYL ACETATE, ASCORBYL PALMITATE, CITRIC ACID.

SKIN LIGHTENING MOISTURIZING LOTION_front

SKIN LIGHTENING MOISTURIZING LOTION_Back

DR. THROWERS SKIN LIGHTENING MOISTURIZING 
hydroquinone lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69299-302
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)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
MINERAL OIL (UNII: T5L8T28FGP)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
CETEARETH-22 (UNII: 28VZG1E234)  
STARCH, POTATO (UNII: 8I089SAH3T)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
TRIMETHYLPENTANEDIOL/ADIPIC ACID/GLYCERIN CROSSPOLYMER (25000 MPA.S) (UNII: 587WKM3S9Q)  
LANOLIN (UNII: 7EV65EAW6H)  
SODIUM METABISULFITE (UNII: 4VON5FNS3C)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
GRAPEFRUIT PEEL (UNII: 3582N05Q44)  
EDETATE SODIUM TETRAHYDRATE (UNII: L13NHD21X6)  
EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
ASCORBYL PALMITATE (UNII: QN83US2B0N)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69299-302-31201 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart358A05/15/2015
Labeler - DR. THROWER'S SKINCARE, INC. (078711495)
Registrant - DR. THROWER'S SKINCARE, INC. (078711495)

Revised: 5/2015
Document Id: b0fb65e3-621d-4c67-b64c-7b06a4bfcf52
Set id: da3da8dc-267d-4d14-a35d-7e0e736bd3d4
Version: 1
Effective Time: 20150522
 
DR. THROWER'S SKINCARE, INC.