Shiseido Future Solution

Manufacturer
SHISEIDO AMERICA INC.
Effective date
2009-12-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:54:30

Label at a glance#

ProductSHISEIDO Future LX Day/Jour
Active ingredientEnsulizole, Octinoxate, Octocrylene
Label structure8 sections

Indications and uses

helps prevent sunburn higher SPF gives more sunburn protection

Dosage and administration

apply smoothly to face before sun exposure and as needed. children under 6 months of age: ask a doctor.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

Active ingredientPurpose
ENSULIZOLE 2%Sunscreen
OCTINOXATE 4.9%Sunscreen
OCTOCRYLENE 5%Sunscreen

Uses

INDICATIONS & USAGE SECTION

  • helps prevent sunburn
  • higher SPF gives more sunburn protection

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

  • keep out of eyes. Rinse with water to remove

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • rash or irritation develops and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

If swallowed, get medical help or contact a Poison'Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • apply smoothly to face before sun exposure and as needed.
  • children under 6 months of age: ask a doctor.

Inactive ingredients

INACTIVE INGREDIENT SECTION

WATER, CYCLOMETHICONE, GLYCERIN, DIPROPYLENE GLYCOL, BEHENYL ALCOHOL, SD ALCOHOL 40-B, DIPHENYLSILOXY PHENYL TRIMETHICONE, SIMMONDSIA CHINENSIS (JOJOBA) SEED OIL, POLYSORBATE 60, DIMETHICONE, GLYCERYL STEARATE, TRIETHANOLAMINE, PEG-20, ERYTHRITOL, PIPERIDINEPROPIONIC ACID, XANTHAN GUM, SACCHAROMYCES FERMENT LYSATE FILTRATE, GLYCINE, ARGININE HCl, MAGNESIUM ASCORBYL PHOSPHATE, SODIUM ACETYLATED HYALURONATE, ONONIS SPINOSA ROOT EXTRACT, AVERRHOA CARAMBOLA LEAF EXTRACT, HIBISCUS ESCULENTUS FRUIT EXTRACT, CAMELLIA SINENSIS LEAF EXTRACT, SODIUM METHYL STEAROYL TAURATE, BUTYLENE GLYCOL, SODIUM CITRATE, SODIUM METAPHOSPHATE, CITRIC ACID, ALCOHOL, BHT, TOCOPHEROL, PHENOXYETHANOL, FRAGRANCE, IRON OXIDES

Questions ?

OTC - QUESTIONS SECTION

1-800-906-7503

PRINCIPAL DISPLAY PANEL - 51g Jar Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SHISEIDO

Future Solution LX

Daytime Protective Cream

SPF 15•PA+

SUNSCREEN

Principal Display Panel - 51g Jar Carton
Principal Display Panel - 51g Jar Carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52686-221-502023-09-26C16284748780-19d75b9d0-afc9-f424-e053-dadaa90a57ceShiseido Future Solution
52686-221-502020-01-31C16284748780-19d75b9d0-afc9-f424-e053-dadaa90a57ceShiseido Future Solution

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
EnsulizoleACTIVE INGREDIENT9YQ9DI1W421
OctinoxateACTIVE INGREDIENT4Y5P7MUD511
OctocryleneACTIVE INGREDIENT5A68WGF6WM1
EnsulizoleACTIVE MOIETY9YQ9DI1W421
OctinoxateACTIVE MOIETY4Y5P7MUD511
OctocryleneACTIVE MOIETY5A68WGF6WM1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52686-22152686-221-50

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
Ensulizole9YQ9DI1W42ACTIB
Octinoxate4Y5P7MUD51ACTIB
Octocrylene5A68WGF6WMACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
4f37ccee-8bc4-42b4-b048-0370d256372781be179f-0952-4198-a526-a4762d15ca342023-09-26WarningsExact identifier
spl set id: 81be179f-0952-4198-a526-a4762d15ca34

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.