FLAWLESS FINISH PERFECTLY NUDE MAKEUP BROAD SPECTRUM SUNSCREEN SPF 15 SHADE COCOA- octinoxate and titanium dioxide lotion 
Elizabeth Arden, 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.

----------

250480

DESCRIPTION

Makeup that feels like your own skin, only better. Light, breathable formula smooths on seamlessly for a naturally luminous look that lasts all day. Minimizes the look of pores and imperfections immediately and over time with continued use. Hydro-pigment color technology, vitamins and antioxidants protect and perfect, so skin looks beautifully even-toned and flawless.

INDICATIONS & USAGE

smooth onto face.

WARNINGS

For external use only

OTC - ACTIVE INGREDIENT

OCTINOXATE 4.00%..............Sunscreen

TITANIUM DIOXIDE 1.26%....Sunscreen

INACTIVE INGREDIENT

WATER/AQUA/EAU, ISOHEXADECANE, HEXYL LAURATE, MICA, GLYCERIN, POLYGLYCERYL-4 ISOSTEARATE, POTASSIUM CETYL PHOSPHATE, CETEARYL ALCOHOL, ASCORBYL PALMITATE, BETAINE, CARBOMER, GLYCERYL STEARATE, HYDROLYZED VEGETABLE PROTEIN, LECITHIN, MAGNESIUM ALUMINUM SILICATE, PEG-100 STEARATE, POLYGLYCERYL-10 MYRISTATE, SODIUM HYDROXIDE, TOCOPHERYL ACETATE, TREMELLA FUCIFORMIS SPOROCARP EXTRACT, CHLORPHENESIN, PHENOXYETHANOL, POTASSIUM SORBATE, SODIUM BENZOATE, SODIUM DEHYDROACETATE [MAY CONTAIN/PEUT CONTENIR (+/-) IRON OXIDES (CI 77491, CI 77492, CI 77499), TITANIUM DIOXIDE (CI 77891).

OTC - DO NOT USE

Do not

use on damaged or broken skin

OTC - KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

OTC - PURPOSE

Provides SPF 15 sun protection.

OTC - STOP USE

Stop use and ask a doctor if rash occurs

OTC - WHEN USING

keep out of eyes. Rinse with water to remove.

FLAWLESS FINISH PERFECTLY NUDE MAKEUP SPF 15

FLAWLESS FINISH PERFECTLY NUDE MAKEUP BROAD SPECTRUM SUNSCREEN SPF 15 SHADE COCOA 
octinoxate and titanium dioxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67938-2027
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE60 mg  in 1500 mg
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE18.9 mg  in 1500 mg
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ISOHEXADECANE (UNII: 918X1OUF1E)  
HEXYL LAURATE (UNII: 4CG9F9W01Q)  
MICA (UNII: V8A1AW0880)  
GLYCERIN (UNII: PDC6A3C0OX)  
POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)  
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)  
ASCORBYL PALMITATE (UNII: QN83US2B0N)  
BETAINE (UNII: 3SCV180C9W)  
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)  
PEG-100 STEARATE (UNII: YD01N1999R)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
CHLORPHENESIN (UNII: I670DAL4SZ)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SODIUM DEHYDROACETATE (UNII: 8W46YN971G)  
Product Characteristics
ColorBROWN (BROWN) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:67938-2027-11 in 1 BOX
1NDC:67938-2027-21500 mg in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35207/17/2013
Labeler - Elizabeth Arden, Inc (849222187)
Establishment
NameAddressID/FEIBusiness Operations
Intercos883457061manufacture(67938-2027)

Revised: 8/2013
Document Id: cedfd055-e137-478d-a327-5287dc10deaa
Set id: e232957f-79aa-4bca-89b9-5d84798071ee
Version: 1
Effective Time: 20130816
 
Elizabeth Arden, Inc