FDA.reportPublic FDA data

SHISEIDO FUTURE LX UNIVERSAL DEFENSE S

Product NDC
58411-902
11-digit product format
584110902
Labeler code
58411
Product ID
58411-902_49732503-4b0d-095d-e063-6294a90a8f4b
Type
HUMAN OTC DRUG
Nonproprietary name
Octisalate, Octocrylene, and Zinc Oxide
Dosage form
CREAM
Route
TOPICAL
Labeler
SHISEIDO AMERICAS CORPORATION
Application
M020
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-01-01
Substance
OCTISALATE; OCTOCRYLENE; ZINC OXIDE
Active strength
1.44; 1.44; 9.7 g/50mL; g/50mL; g/50mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product
Yes
Brand name base
SHISEIDO FUTURE LX UNIVERSAL DEFENSE S
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
OCTISALATE1.44 g/50mL
OCTOCRYLENE1.44 g/50mL
ZINC OXIDE9.7 g/50mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 3 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
4X49Y0596WInternal UNII lookup
5A68WGF6WMInternal UNII lookup
SOI2LOH54ZInternal UNII lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
0a6f8eef-48e9-44f5-9811-629bc0dc07d0Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58411-902-60SHISEIDO FUTURE LX UNIVERSAL DEFENSE S50 mL in 1 TUBECREAM502
58411-902-60SHISEIDO FUTURE LX UNIVERSAL DEFENSE S1 in 1 CARTONCREAM12

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 128 of 354 · 7,077 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Daily Mineral ProtectionZINC OXIDECharisma Skin352dc69b-86d0-aa15-e063-6294a90a5e4c2025-12-12Exact identifier
application number: M020
Ultra Sheer SunscreenZINC OXIDESKINBAR MD LLC35810a90-e2ca-b80b-e063-6294a90a14f02025-12-12Exact identifier
application number: M020
Tinted Facial Mineral Sunscreen SPF 40TITANIUM DIOXIDE, ZINC OXIDERSL89 LLC3531d609-a0d8-cb59-e063-6394a90a4bea2025-12-12Exact identifier
application number: M020
Non-Tinted Zinc Body And Face SPF40ZINC OXIDERSL89 LLC3532102c-8ded-1e78-e063-6294a90ae2242025-12-12Exact identifier
application number: M020
Non-Tinted Zinc Body And Face SPF40ZINC OXIDERSL89 LLC35330a82-dc6b-49af-e063-6394a90af9ea2025-12-12Exact identifier
application number: M020
Tinted Replenishing SPF40ZINC OXIDERSL89 LLC353257db-6c30-4a03-e063-6294a90ae45d2025-12-12Exact identifier
application number: M020
Tinted Facial Mineral Sunscreen SPF 40TITANIUM DIOXIDE, ZINC OXIDERSL89 LLC3532a6a2-dbb5-8111-e063-6294a90aeaeb2025-12-12Exact identifier
application number: M020
Tinted Replenishing SPF40ZINC OXIDERSL89 LLC35334c75-b3fd-37fa-e063-6294a90ab3b02025-12-12Exact identifier
application number: M020
Age Defying SunscreenZINC OXIDEGINAMARIE Products35835565-f10b-e8e7-e063-6394a90ab2d32025-12-12Exact identifier
application number: M020
Tinted Daily Mineral SunscreenTITANIUM DIOXIDE, ZINC OXIDERSL89 LLC35338026-525a-d8b3-e063-6394a90a98f52025-12-12Exact identifier
application number: M020
Mineral Lip ProtectionTITANIUM DIOXIDE, ZINC OXIDERSL89 LLC3541971e-3664-a9f5-e063-6294a90ac2d22025-12-12Exact identifier
application number: M020
Age Defying SunscreenZINC OXIDEGINAMARIE Products35837cf7-91e5-f9ec-e063-6394a90aa91e2025-12-12Exact identifier
application number: M020
Mineral Sunscreen Face plus BodyZINC OXIDEKS Esthetics, LLC390a4d8d-b47f-0d9a-e063-6394a90a9b532025-12-12Exact identifier
application number: M020
Mineral Sunscreen Tinted Zinc OxideZINC OXIDEKS Esthetics, LLC3909e657-97a5-dd3c-e063-6394a90a10eb2025-12-12Exact identifier
application number: M020
Prime Protection Sunscreen non tintedTITANIUM DIOXIDE, ZINC OXIDEKRISTI REDD ESTHETICS36608832-22d8-bc76-e063-6394a90abac62025-12-12Exact identifier
application number: M020
Prime Protection Sunscreen, tintedTITANIUM DIOXIDE, ZINC OXIDEKRISTI REDD ESTHETICS3660af9e-d60f-c33e-e063-6394a90a3a052025-12-12Exact identifier
application number: M020
Hydrating Antioxidant Sunscreen tintedZINC OXIDEKRISTI REDD ESTHETICS366149e2-b03c-e798-e063-6394a90a6a1d2025-12-12Exact identifier
application number: M020
Prime Protection Sunscreen, tintedTITANIUM DIOXIDE, ZINC OXIDEKRISTI REDD ESTHETICS3660e701-1373-eef4-e063-6394a90a61402025-12-12Exact identifier
application number: M020
Hydrating Antioxidant Sunscreen tintedZINC OXIDEKRISTI REDD ESTHETICS3661251d-b907-8df6-e063-6294a90a1c732025-12-12Exact identifier
application number: M020
sheer tinted sunscreenTITANIUM DIOXIDE, ZINC OXIDESARA ELIZABETH SKINCARE3b177c49-ed8c-42b9-e063-6294a90a82c62025-12-12WarningsExact identifier
application number: M020

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
58411-902-60584110902601 TUBE in 1 CARTON (58411-902-60) / 50 mL in 1 TUBE1 tube2025-01-01NoNoCurrent