SHISEIDO BENEFIANCE WRINKLERESIST24 DAY- avobenzone, octinoxate, and octocrylene 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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SHISEIDO BENEFIANCE WRINKLERESIST24 DAY EMULSION

Drug Facts

Active ingredientsPurpose
AVOBENZON 2.5 %Sunscreen
OCTINOXATE 7.4 %Sunscreen
OCTOCRYLENE 2.0 % 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.

Directions

For sunscreen use:

Inactive Ingredients

WATER•GLYCERIN•SD ALCOHOL 40-B•DIPROPYLENE GLYCOL•XYLITOL•BUTYLENE GLYCOL•SILICA•POLYBUTYLENE GLYCOL/PPG-9/1 COPOLYMER•HYDROGENATED POLYDECENE•PEG-60 GLYCERYL ISOSTEARATE•TRIISOSTEARIN•DIMETHICONE•DIPHENYLSILOXY PHENYL TRIMETHICONE•XANTHAN GUM•PEG/PPG-17/4 DIMETHYL ETHER•PHYTOSTERYL MACADAMIATE•TOCOPHERYL ACETATE•SAPINDUS MUKUROSSI PEEL EXTRACT•UNCARIA GAMBIR EXTRACT•SODIUM ACETYLATED HYALURONATE•HYDROXYPROLINE•THYMUS SERPILLUM EXTRACT•CHLORELLA VULGARIS EXTRACT•STEARIC ACID•GLYCERYL STEARATE SE•BEHENYL ALCOHOL•ISOSTEARIC ACID•BEHENIC ACID•BEHENETH-20•TRIETHANOLAMINE•CELLULOSE GUM•DISODIUM EDTA•SODIUM METAPHOSPHATE•ALCOHOL•BHT•TOCOPHEROL•PHENOXYETHANOL•FRAGRANCE•IRON OXIDES•

Other information

Protect this product in this container from excessive heat and direct sun.

Questions or comments?

Call toll free 1-800-906-7503

PRINCIPAL DISPLAY PANEL - 75 mL Bottle Carton

SHISEIDO

BENEFIANCE

WrinkleResist24

Day Emulsion

BROAD SPECTRUM
SPF 18
SUNSCREEN

75mL 2.5 FL. OZ.

Principal Display Panel - 75 mL Bottle Carton
SHISEIDO BENEFIANCE WRINKLERESIST24 DAY 
avobenzone, octinoxate, and octocrylene emulsion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58411-628
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE1.94 g  in 75 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE5.83 g  in 75 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE1.55 g  in 75 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
DIPROPYLENE GLYCOL (UNII: E107L85C40)  
XYLITOL (UNII: VCQ006KQ1E)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
HYDROGENATED POLYDECENE TYPE I (UNII: U333RI6EB7)  
PEG-60 GLYCERYL ISOSTEARATE (UNII: WQP0973914)  
TRIISOSTEARIN (UNII: 71503RH8KG)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
DIPHENYLSILOXY PHENYL TRIMETHICONE (UNII: I445L28B12)  
XANTHAN GUM (UNII: TTV12P4NEE)  
PEG/PPG-17/4 DIMETHYL ETHER (UNII: 4ET18WJG5K)  
PHYTOSTERYL MACADAMIATE (UNII: 233VSF903M)  
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)  
SAPINDUS MUKOROSSI FRUIT RIND (UNII: 3D1P12PN9U)  
UNCARIA GAMBIR WHOLE (UNII: K63NT5I1B8)  
SODIUM ACETYLATED HYALURONATE (UNII: WN66R7GL93)  
HYDROXYPROLINE (UNII: RMB44WO89X)  
CHLORELLA VULGARIS (UNII: RYQ4R60M02)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
DOCOSANOL (UNII: 9G1OE216XY)  
ISOSTEARIC ACID (UNII: X33R8U0062)  
BEHENIC ACID (UNII: H390488X0A)  
BEHENETH-20 (UNII: BJ4GP2IFLN)  
TROLAMINE (UNII: 9O3K93S3TK)  
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
SODIUM POLYMETAPHOSPHATE (UNII: P1BM4ZH95L)  
ALCOHOL (UNII: 3K9958V90M)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:58411-628-101 in 1 CARTON01/01/2021
175 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart35201/01/2021
Labeler - SHISEIDO AMERICAS CORPORATION (193691821)

Revised: 2/2021
Document Id: ca3efed4-cea4-4fc2-94ad-a6a4d8922c22
Set id: d308d578-c881-4c10-8c79-9e3cd58b694c
Version: 1
Effective Time: 20210225
 
SHISEIDO AMERICAS CORPORATION