LA MER

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
2010-04-29
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 22:24:21

Label at a glance#

ProductLA MER THE SPF 30 UV PROTECTING FLUID
Active ingredientZINC OXIDE, OCTINOXATE
Label structure3 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS: ZINC OXIDE 10.00% [] OCTINOXATE 7.50%

WARNINGS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PRINCIPALDISPLAY PANEL:

fluid de la mer

LA MER
THE SPF 30

UV PROTECTING FLUID



1.4 FL. OZ. LIQ. / 40 ML




MAX HUBER RESEARCH LAB, DIST
NEW YORK, NY 10022


FOLDING CARTON
FOLDING CARTON

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
65966-009-012020-01-31C16284748780-19d75b9d0-e1e2-f424-e053-dadaa90a57ceceec72b2-ed8b-4934-ae7a-7a53bd24d170

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
65966-009-01LA MER THE SPF 30 UV PROTECTING FLUID1 in 1 CARTONLIQUID13
65966-009-02LA MER THE SPF 30 UV PROTECTING FLUID40 mL in 1 BOTTLE, PLASTICLIQUID403

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
65966-009LA MER (ZINC OXIDE, OCTINOXATE) LIQUID [MAX HUBER RESEARCH LAB INC]3Legacy NDC, 2 package rows20100430_ceec72b2-ed8b-4934-ae7a-7a53bd24d170.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD513
ZINC OXIDEACTIVE INGREDIENTSOI2LOH54Z3
OCTINOXATEACTIVE MOIETY4Y5P7MUD513
ZINC OXIDEACTIVE MOIETYSOI2LOH54Z3

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
65966-00965966-009-02, 65966-009-01

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
ZINC OXIDESOI2LOH54ZACTIB
OCTINOXATE4Y5P7MUD51ACTIB

Source Document#

Source XML · Source PDF

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
56070748-6ce4-4c1b-826c-d704245d9528ceec72b2-ed8b-4934-ae7a-7a53bd24d1702010-04-29WarningsExact identifier
spl id: 56070748-6ce4-4c1b-826c-d704245d9528
spl set id: ceec72b2-ed8b-4934-ae7a-7a53bd24d170

Reported adverse events (FAERS/openFDA)#

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