FUTURIST AGE RESISTING MAKEUP

Manufacturer
ESTEE LAUDER INC | ESTEE LAUDER COSMETICS, LTD | ESTEE LAUDER N.V. | Len-Ron Manufacturing Division of Aramis Inc. | Aramis Inc. | Northtec Bristol | Northtec Keystone | PADC 1 | Estee Lauder Pennsylvania Distribution Center 2 | Estee Lauder Cosmetics, Ltd. | Estee Lauder Cosmetics Distribution Center | Estee Lauder Kabushiki Kaisha | Whitman Laboratories Ltd. | Aveda Corporation
Effective date
2010-04-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:24:10

Label at a glance#

ProductFUTURIST AGE RESISTING MAKEUP SPF 15
Active ingredientOCTINOXATE
Label structure4 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENT: OCTINOXATE 2.2%

WARNINGS SECTION

WARNING: KEEP OUT OF EYES. STOP USE IF IRRITATION OCCURS.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION


KEEP OUT OF REACH OF CHILDREN

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

 

PRINCIPAL DISPLAY PANEL

ESTEE LAUDER

FUTURIST

AGE-RESISTING MAKEUP

SPF 15


1 FL 0Z / 30 ML

ESTEE LAUDER DIST

NEW YORK, NY 10022


FOLDING CARTONFOLDING CARTON

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11559-003-012019-10-21C16284748780-1956f9ecf-cfd5-621f-e053-dbdaa90a74ad076caf65-e4ba-4ce2-a7aa-10228179a50c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11559-003-01FUTURIST AGE RESISTING MAKEUPSPF 151 in 1 CARTONLIQUID11
11559-003-02FUTURIST AGE RESISTING MAKEUPSPF 1530 mL in 1 TUBELIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11559-003FUTURIST AGE RESISTING MAKEUP SPF 15 (TITANIUM DIOXIDE) LIQUID [ESTEE LAUDER INC]1Legacy NDC, 2 package rows20100406_076caf65-e4ba-4ce2-a7aa-10228179a50c.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD511
OCTINOXATEACTIVE MOIETY4Y5P7MUD511

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
11559-00311559-003-02, 11559-003-01

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
OCTINOXATE4Y5P7MUD51ACTIB

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
64f94403-12d6-475a-8c97-fe164f4e2da9076caf65-e4ba-4ce2-a7aa-10228179a50c2010-04-06WarningsExact identifier
spl id: 64f94403-12d6-475a-8c97-fe164f4e2da9
spl set id: 076caf65-e4ba-4ce2-a7aa-10228179a50c

Reported adverse events (FAERS/openFDA)#

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