SHISEIDO BENEFIANCE WRINKLERESIST24 DAY- avobenzone, octinoxate, and octocrylene cream 
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 CREAM

Drug Facts

Active ingredients            Purpose
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∙DIPROPYLENE GLYCOL∙BUTYLENE GLYCOL∙PHENYL TRIMETHICONE∙HYDROGENATED POLYDECENE∙SORBITOL∙MYRISTYL MYRISTATE∙DIMETHICONE∙SD ALCOHOL 40-B∙POLYBUTYLENE GLYCOL/PPG-9/1 COPOLYMER∙PETROLATUM∙STEARYL ALCOHOL∙STEARIC ACID∙SILICA∙BENTONITE∙PALMITIC ACID∙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∙PEG-5 GLYCERYL STEARATE∙GLYCERYL STEARATE SE∙TRISODIUM EDTA∙POTASSIUM HYDROXIDE∙SODIUM METAPHOSPHATE∙AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER∙ALCOHOL∙SODIUM METABISULFITE∙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 - 50 mL Bottle Carton

SHISEIDO

BENEFIANCE
WrinkleResist24
Day Cream
BROAD SPECTRUM
SPF 18
SUNSCREEN

50mL NET WT. 1.8 OZ.

PRINCIPAL DISPLAY PANEL - 50 mL Bottle Carton
SHISEIDO BENEFIANCE WRINKLERESIST24 DAY 
avobenzone, octinoxate, and octocrylene cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58411-629
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE1.28 g  in 50 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE3.85 g  in 50 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE1.02 g  in 50 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
DIPROPYLENE GLYCOL (UNII: E107L85C40)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)  
HYDROGENATED POLYDECENE TYPE I (UNII: U333RI6EB7)  
SORBITOL (UNII: 506T60A25R)  
MYRISTYL MYRISTATE (UNII: 4042ZC00DY)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
PETROLATUM (UNII: 4T6H12BN9U)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
BENTONITE (UNII: A3N5ZCN45C)  
PALMITIC ACID (UNII: 2V16EO95H1)  
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)  
SODIUM ACETYLATED HYALURONATE (UNII: WN66R7GL93)  
HYDROXYPROLINE (UNII: RMB44WO89X)  
CHLORELLA VULGARIS (UNII: RYQ4R60M02)  
PEG-5 GLYCERYL STEARATE (UNII: 8CAC4NQ872)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
EDETATE TRISODIUM (UNII: 420IP921MB)  
POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
SODIUM POLYMETAPHOSPHATE (UNII: P1BM4ZH95L)  
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)  
ALCOHOL (UNII: 3K9958V90M)  
SODIUM METABISULFITE (UNII: 4VON5FNS3C)  
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:58411-629-101 in 1 CARTON01/01/2021
150 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: 93ef9789-3ddd-47a0-bb67-7fdda500da36
Set id: 7d9c0f81-005f-4223-940e-a64143db5275
Version: 1
Effective Time: 20210225
 
SHISEIDO AMERICAS CORPORATION