SHISEIDO FUTURE SOLUTION LX TOTAL PROTECTIVE E- avobenzone, octinoxate, octocrylene, and oxybenzone 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 FUTURE SOLUTION LX TOTAL PROTECTIVE E

Drug Facts

Active ingredientsPurpose
AVOBENZONE 2.0%Sunscreen
OCTINOXATE 7.4%Sunscreen
OCTOCRYLENE 3.0%Sunscreen
OXYBENZONE 1.5%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∙BEHENYL ALCOHOL∙BUTYLENE GLYCOL∙ISOHEXADECANE∙SD ALCOHOL 40-B∙SILICA∙CAPRYLIC/CAPRIC TRIGLYCERIDE∙MYRISTYL MYRISTATE∙DIMETHICONE∙POLYBUTYLENE GLYCOL/PPG-9/1 COPOLYMER∙SORBITOL∙STEARYL ALCOHOL∙PHYTOSTERYL MACADAMIATE∙TOCOPHERYL ACETATE∙PEG/PPG-17/4 DIMETHYL ETHER∙PIPERIDINEPROPIONIC ACID∙2-O-ETHYL ASCORBIC ACID∙PRUNUS SPECIOSA LEAF EXTRACT∙ANGELICA ACUTILOBA ROOT EXTRACT∙ISODONIS JAPONICUS LEAF/STALK EXTRACT∙CAMELLIA SINENSIS LEAF EXTRACT∙ZANTHOXYLUM PIPERITUM PEEL EXTRACT∙BEHENETH-20∙SUCCINOGLYCAN∙TRISODIUM EDTA∙SODIUM CITRATE∙ALCOHOL∙BHT∙SODIUM METAPHOSPHATE∙CITRIC ACID∙TALC∙DEXTRIN PALMITATE∙TOCOPHEROL∙METHYLPARABEN∙ETHYLPARABEN∙FRAGRANCE∙IRON OXIDES∙

Other information

Questions or comments?

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PRINCIPAL DISPLAY PANEL - 50 mL Jar Carton

SHISEIDO
GINZA TOKYO

FUTURE SOLUTION LX

Total Protective Cream

SkingenecellEnmei

BROAD SPECTRUM SPF 20
SUNSCREEN

50mL NET WT. 1.7 OZ.

PRINCIPAL DISPLAY PANEL - 50 mL Jar Carton
SHISEIDO FUTURE SOLUTION LX TOTAL PROTECTIVE E 
avobenzone, octinoxate, octocrylene, and oxybenzone cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58411-328
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE1017 mg  in 50 mL
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE3763 mg  in 50 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE1526 mg  in 50 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE763 mg  in 50 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
DIPROPYLENE GLYCOL (UNII: E107L85C40)  
DOCOSANOL (UNII: 9G1OE216XY)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
ISOHEXADECANE (UNII: 918X1OUF1E)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
MYRISTYL MYRISTATE (UNII: 4042ZC00DY)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
SORBITOL (UNII: 506T60A25R)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
PHYTOSTERYL MACADAMIATE (UNII: 233VSF903M)  
.ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)  
PEG/PPG-17/4 DIMETHYL ETHER (UNII: 4ET18WJG5K)  
PIPERIDINEPROPIONIC ACID (UNII: 6L69A7VPHO)  
2-O-ETHYL ASCORBIC ACID (UNII: 801M14RK9K)  
PRUNUS SPECIOSA LEAF (UNII: Q71D900FVU)  
ANGELICA ACUTILOBA ROOT (UNII: 3W51R3EK30)  
GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
ZANTHOXYLUM PIPERITUM FRUIT RIND (UNII: 728JDI7G4M)  
BEHENETH-20 (UNII: BJ4GP2IFLN)  
EDETATE TRISODIUM (UNII: 420IP921MB)  
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
ALCOHOL (UNII: 3K9958V90M)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
SODIUM POLYMETAPHOSPHATE (UNII: P1BM4ZH95L)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
TALC (UNII: 7SEV7J4R1U)  
DEXTRIN PALMITATE (CORN; 20000 MW) (UNII: 89B2BSF9I3)  
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
ETHYLPARABEN (UNII: 14255EXE39)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:58411-328-501 in 1 CARTON08/01/2017
150 mL in 1 JAR; Type 0: Not a Combination Product
2NDC:58411-328-511 in 1 CARTON05/01/2021
230 mL in 1 JAR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35208/01/2017
Labeler - SHISEIDO AMERICAS CORPORATION (193691821)
Establishment
NameAddressID/FEIBusiness Operations
SHISEIDO AMERICA INC.782677132manufacture(58411-328) , analysis(58411-328)

Revised: 3/2021
Document Id: 2668be02-92ec-4cff-b6de-55d103544607
Set id: b233ddca-83f8-426f-8d52-eac93ab239ec
Version: 3
Effective Time: 20210326
 
SHISEIDO AMERICAS CORPORATION