Label: SHISEIDO FUTURE SOLUTION LX TOTAL PROTECTIVE- avobenzone, octinoxate, octocrylene, and oxybenzone emulsion
- NDC Code(s): 58411-327-10
- Packager: SHISEIDO AMERICAS CORPORATION
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 5, 2026
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
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Uses
- helps prevent sunburn
- if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun
- Warnings
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Directions
For sunscreen use:
- apply liberally 15 minutes before sun exposure
- use a water resistant sunscreen if swimming or sweating
- reapply at least every 2 hours
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Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a broad spectrum SPF of 15 or higher and other sun protection measures including:
- limit time in the sun, especially from 10 a.m. – 2 p.m.
- wear long-sleeve shirts, pants, hats, and sunglasses
- children under 6 months: Ask a doctor
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Inactive Ingredients
WATER∙DIPROPYLENE GLYCOL∙SD ALCOHOL 40-B∙GLYCERIN∙HYDROGENATED POLYDECENE∙XYLITOL∙ISODODECANE∙DIMETHICONE∙PEG-5 GLYCERYL STEARATE∙ISOSTEARIC ACID∙SILICA∙PHENYL TRIMETHICONE∙TRIETHANOLAMINE∙XANTHAN GUM∙TOCOPHERYL ACETATE∙PEG/PPG-17/4 DIMETHYL ETHER∙PIPERIDINEPROPIONIC ACID∙PHYTOSTERYL MACADAMIATE∙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∙PPG-17∙GLYCERYL STEARATE SE∙BEHENYL ALCOHOL∙BEHENIC ACID∙STEARIC ACID∙BATYL ALCOHOL∙PEG-30 PHYTOSTEROL∙BUTYLENE GLYCOL∙CARBOMER∙DISODIUM EDTA∙ALCOHOL∙BHT∙CELLULOSE GUM∙SODIUM METAPHOSPHATE∙TALC∙DEXTRIN PALMITATE∙TOCOPHEROL∙ETHYLPARABEN∙METHYLPARABEN∙FRAGRANCE∙IRON OXIDES∙
- Other information
- Questions or comments?
- PRINCIPAL DISPLAY PANEL - 75 mL Bottle Carton
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INGREDIENTS AND APPEARANCE
SHISEIDO FUTURE SOLUTION LX TOTAL PROTECTIVE
avobenzone, octinoxate, octocrylene, and oxybenzone emulsionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:58411-327 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 1136 mg in 75 mL OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 5606 mg in 75 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 1515 mg in 75 mL OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 758 mg in 75 mL Inactive Ingredients Ingredient Name Strength PIPERIDINEPROPIONIC ACID (UNII: 6L69A7VPHO) PHYTOSTERYL MACADAMIATE (UNII: 233VSF903M) 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) PPG-17 (UNII: OV0Q322E0U) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) DOCOSANOL (UNII: 9G1OE216XY) BEHENIC ACID (UNII: H390488X0A) STEARIC ACID (UNII: 4ELV7Z65AP) BATILOL (UNII: 39YR661C4U) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) EDETATE DISODIUM (UNII: 7FLD91C86K) ALCOHOL (UNII: 3K9958V90M) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311) SODIUM POLYMETAPHOSPHATE (UNII: P1BM4ZH95L) TALC (UNII: 7SEV7J4R1U) DEXTRIN PALMITATE (CORN; 20000 MW) (UNII: 89B2BSF9I3) .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1) ETHYLPARABEN (UNII: 14255EXE39) METHYLPARABEN (UNII: A2I8C7HI9T) FERRIC OXIDE RED (UNII: 1K09F3G675) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) WATER (UNII: 059QF0KO0R) DIPROPYLENE GLYCOL (UNII: E107L85C40) GLYCERIN (UNII: PDC6A3C0OX) HYDROGENATED POLYDECENE TYPE I (UNII: U333RI6EB7) XYLITOL (UNII: VCQ006KQ1E) ISODODECANE (UNII: A8289P68Y2) DIMETHICONE (UNII: 92RU3N3Y1O) PEG-5 GLYCERYL STEARATE (UNII: 8CAC4NQ872) ISOSTEARIC ACID (UNII: X33R8U0062) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R) TROLAMINE (UNII: 9O3K93S3TK) XANTHAN GUM (UNII: TTV12P4NEE) .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8) PEG/PPG-17/4 DIMETHYL ETHER (UNII: 4ET18WJG5K) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:58411-327-10 1 in 1 CARTON 08/01/2017 1 75 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 08/01/2017 Labeler - SHISEIDO AMERICAS CORPORATION (193691821) Establishment Name Address ID/FEI Business Operations Shiseido America Inc. 782677132 analysis(58411-327) , manufacture(58411-327)

