CLE DE PEAU BEAUTE BRIGHTENING ENHANCER VEIL- octinoxate, octocrylene, and titanium dioxide emulsion 
SHISEIDO AMERICAS CORPORATION

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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clé de peau BEAUTÉ BRIGHTENING ENHANCER VEIL

Drug Facts

Active ingredientsPurpose
Octinoxate 7.4%Sunscreen
Octocrylene 2.5%Sunscreen
Titanium Dioxide 6.6%Sunscreen

Uses

Warnings

For external use only

Do not use on damaged or broken skin

When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if rash occurs.

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

Flammable: Do not use near heat, flame, or while smoking.

Directions

For sunscreen use:

Inactive Ingredients

WATER•DIMETHICONE•TRISILOXANE•BUTYLENE GLYCOL•GLYCERIN•ISOPROPYL MYRISTATE•SD ALCOHOL 40-B•PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE•SILICA•BARIUM SULFATE•POTASSIUM METHOXYSALICYLATE•TREHALOSE•HYDROGENATED POLYISOBUTENE•SODIUM POLYACRYLATE•TOCOPHERYL ACETATE•GLYCINE•CAMELLIA SINENSIS LEAF EXTRACT•PEG/PPG-14/7 DIMETHYL ETHER•ROSA ROXBURGHII FRUIT EXTRACT•ANGELICA ACUTILOBA ROOT EXTRACT•HYDROLYZED CONCHIOLIN PROTEIN•HYDROLYZED SILK•PERILLA OCYMOIDES LEAF EXTRACT•PPG-17•ALUMINUM HYDROXIDE•DISTEARDIMONIUM HECTORITE•HYDROGEN DIMETHICONE•STEARIC ACID•TRISODIUM EDTA•BUTYROSPERMUM PARKII (SHEA) BUTTER•CITRIC ACID•SODIUM CITRATE•ALCOHOL•TALC•BHT•TOCOPHEROL•SODIUM METABISULFITE•POLYSILICONE-2•THEANINE•BIS-BUTYLDIMETHICONE POLYGLYCERYL-3•PHENOXYETHANOL•FRAGRANCE•TITANIUM DIOXIDE•IRON OXIDES•

Other information

Questions or comments?

Call toll free 1-800-906-7503

PRINCIPAL DISPLAY PANEL - 30 mL Bottle Box

clé de peau
BEAUTÉ

BRIGHTENING
ENHANCER VEIL

BROAD SPECTRUM
SPF 32
SUNSCREEN

30mL 1 FL. OZ.

PRINCIPAL DISPLAY PANEL - 30 mL Bottle Box
CLE DE PEAU BEAUTE BRIGHTENING ENHANCER VEIL 
octinoxate, octocrylene, and titanium dioxide emulsion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58411-838
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE2220 mg  in 30 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE750 mg  in 30 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE1980 mg  in 30 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
TRISILOXANE (UNII: 9G1ZW13R0G)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
GLYCERIN (UNII: PDC6A3C0OX)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: 25G622K2RA)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
BARIUM SULFATE (UNII: 25BB7EKE2E)  
POTASSIUM METHOXYSALICYLATE (UNII: 5G3H7U4Y7F)  
TREHALOSE (UNII: B8WCK70T7I)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
GLYCINE (UNII: TE7660XO1C)  
GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
PEG/PPG-14/7 DIMETHYL ETHER (UNII: 6DNW9T7YT2)  
ROSA ROXBURGHII FRUIT (UNII: CVT1AA87FF)  
ANGELICA ACUTILOBA ROOT (UNII: 3W51R3EK30)  
PERILLA FRUTESCENS LEAF (UNII: T4L5881Y68)  
PPG-17 (UNII: OV0Q322E0U)  
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
EDETATE TRISODIUM (UNII: 420IP921MB)  
SHEA BUTTER (UNII: K49155WL9Y)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
ALCOHOL (UNII: 3K9958V90M)  
TALC (UNII: 7SEV7J4R1U)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
TOCOPHEROL (UNII: R0ZB2556P8)  
SODIUM METABISULFITE (UNII: 4VON5FNS3C)  
THEANINE (UNII: 8021PR16QO)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:58411-838-101 in 1 BOX04/01/2022
130 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 finalpart35204/01/2022
Labeler - SHISEIDO AMERICAS CORPORATION (193691821)

Revised: 5/2022
Document Id: 132674e9-a0c0-4135-9b0c-0cb829f387a0
Set id: bb00d6d7-cc51-4fee-a0df-68bbd5bc50d6
Version: 1
Effective Time: 20220512
 
SHISEIDO AMERICAS CORPORATION