SHISEIDO BENEFIANCE NUTRIPERFECT 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 NUTRIPERFECT DAY

Drug Facts

ACTIVE INGREDIENTS:Purpose
AVOBENZONE 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, BUTYLENE GLYCOL, GLYCERIN, DIPROPYLENE GLYCOL, DIMETHICONE, GLYCERYL STEARATE SE, BEHENYL ALCOHOL, PEG/PPG-14/7 DIMETHYL ETHER, POLYBUTYLENE GLYCOL/PPG-9/1 COPOLYMER, HYDROGENATED POLYDECENE, ISOPROPYL MYRISTATE, MYRISTYL MYRISTATE, MICROCRYSTALLINE WAX, PEG-40 STEARATE, SILICA, CARNOSINE, XANTHAN GUM, ERYTHRITOL, TOCOPHERYL ACETATE, POTASSIUM ASCORBYL TOCOPHERYL PHOSPHATE, PANTHENYL ETHYL ETHER, SODIUM ACETYLATED HYALURONATE, SORBITAN TRISTEARATE, STEARYL ALCOHOL, CELLULOSE GUM, SODIUM METAPHOSPHATE, TRISODIUM EDTA, BHT, SODIUM METABISULFITE, TOCOPHEROL, PHENOXYETHANOL, FRAGRANCE, IRON OXIDES,

Other information

Questions or comments?

Call toll free 1-800-906-7503

SHISEIDO AMERICA INC.
NEW YORK, N.Y. 10022
SHISEIDO DIST.
NEW YORK • PARIS • MILANO

PRINCIPAL DISPLAY PANEL - 50 mL Jar Carton

SHISEIDO

BENEFIANCE
NutriPerfect

Day Cream

BROAD SPECTRUM
SPF 18

SUNSCREEN

PRO-FORTIFYING
Carnosine DP™

50mL NET WT. 1.8 OZ.

PRINCIPAL DISPLAY PANEL - 50 mL Jar Carton
SHISEIDO BENEFIANCE NUTRIPERFECT DAY 
avobenzone, octinoxate, and octocrylene cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58411-351
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE1286 mg  in 51.45 g
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE3807 mg  in 51.45 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE1029 mg  in 51.45 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
GLYCERIN (UNII: PDC6A3C0OX)  
DIPROPYLENE GLYCOL (UNII: E107L85C40)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
DOCOSANOL (UNII: 9G1OE216XY)  
PEG/PPG-14/7 DIMETHYL ETHER (UNII: 6DNW9T7YT2)  
HYDROGENATED POLYDECENE (550 MW) (UNII: U333RI6EB7)  
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
MYRISTYL MYRISTATE (UNII: 4042ZC00DY)  
PEG-40 STEARATE (UNII: ECU18C66Q7)  
CARNOSINE (UNII: 8HO6PVN24W)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
SORBITAN TRISTEARATE (UNII: 6LUM696811)  
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
XANTHAN GUM (UNII: TTV12P4NEE)  
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)  
SODIUM POLYMETAPHOSPHATE (UNII: P1BM4ZH95L)  
ERYTHRITOL (UNII: RA96B954X6)  
EDETATE TRISODIUM (UNII: 420IP921MB)  
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)  
PANTHENYL ETHYL ETHER (UNII: F4WMF8NX3B)  
POTASSIUM ASCORBYL TOCOPHERYL PHOSPHATE (UNII: 61R4GJ48ER)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
SODIUM METABISULFITE (UNII: 4VON5FNS3C)  
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:58411-351-501 in 1 CARTON11/01/2012
151.45 g in 1 JAR; Type 0: Not a Combination Product
2NDC:58411-351-511 in 1 CARTON11/01/2012
24.12 g in 1 JAR; Type 0: Not a Combination Product
3NDC:58411-351-521 in 1 CARTON11/01/2012
310.29 g in 1 JAR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart35211/01/2012
Labeler - SHISEIDO AMERICAS CORPORATION (193691821)
Establishment
NameAddressID/FEIBusiness Operations
SHISEIDO AMERICA INC.782677132MANUFACTURE(58411-351) , ANALYSIS(58411-351)

Revised: 12/2019
Document Id: 871fa8a1-03db-49fa-b195-e6919002fbc6
Set id: f644c67b-3a71-411b-b321-39a8b18af0c7
Version: 2
Effective Time: 20191227
 
SHISEIDO AMERICAS CORPORATION