FDA.reportPublic FDA data

LA MER THE TREATMENT FLUID FOUNDATION

Manufacturer
MAX HUBER RESEARCH LAB 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
2010-04-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:24:09

Label at a glance#

ProductLA MER THE TREATMENT FLUID FOUNDATION SPF 15
Active ingredientTITANIUM DIOXIDE, OCTINOXATE
Label structure4 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS: TITANIUM DIOXIDE 4.7%, OCTINOXATE 2.2%

WARNINGS SECTION

WARNING: KEEP OUT OF EYES. IF IRRITATION PERSISTS, CONSULT A HEALTH CARE PRACTITIONER. KEEP OUT OF REACH OF CHILDREN.

OTC - WHEN USING SECTION

DIRECTIONS: APPLY PRIOR TO SUN EXPOSURE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL  


LA MER

THE TREATMENT FLUID FOUNDATION

SPF 15

1.0 FL OZ/30 mL


MAX HUBER RESEARCH LAB INC.

NEW YORK, NY 10022

FOLDING CARTONFOLDING CARTON

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
65966-001-012020-01-31C16284748780-19d75b9d0-70bd-f424-e053-dadaa90a57ce2661709d-74d5-4a21-8919-a087404c7423

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
65966-001-01LA MER THE TREATMENT FLUID FOUNDATIONSPF 151 in 1 CARTONLIQUID11
65966-001-02LA MER THE TREATMENT FLUID FOUNDATIONSPF 1530 mL in 1 TUBELIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
65966-001LA MER THE TREATMENT FLUID FOUNDATION SPF 15 (TITANIUM DIOXIDE OCTINOXATE) LIQUID [MAX HUBER RESEARCH LAB INC]1Legacy NDC, 2 package rows20100405_2661709d-74d5-4a21-8919-a087404c7423.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD511
TITANIUM DIOXIDEACTIVE INGREDIENT15FIX9V2JP1
OCTINOXATEACTIVE MOIETY4Y5P7MUD511
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP1

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
65966-00165966-001-02, 65966-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
TITANIUM DIOXIDE15FIX9V2JPACTIB
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
edabc2ce-e1c0-4db5-9d14-46294e20d2312661709d-74d5-4a21-8919-a087404c74232010-04-02WarningsExact identifier
spl id: edabc2ce-e1c0-4db5-9d14-46294e20d231
spl set id: 2661709d-74d5-4a21-8919-a087404c7423

Reported adverse events (FAERS/openFDA)#

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