FDA.reportPublic FDA data

DAYWEAR PLUS MULTI PROTECTION TINTED MOISTURIZER

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
2010-04-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:24:13

Label at a glance#

ProductDAYWEAR PLUS MULTI PROTECTION TINTED MOISTURIZER SPF 15
Active ingredientOCTINOXATE, OCTISALATE, AVOBENZONE
Label structure3 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS: OCTINOXATE 7.50% [] OCTISALATE 5.00% [] AVOBENZONE 2.00%

WARNINGS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

DAY WEAR PLUS

MULTI PROTECTION

TINTED MOISTURIZER

SPF 15

All Skintypes

1.7 FL OZ LIQ/ 50 ML

ESTEE LAUDER DIST.

NEW YORK, NY 10022

9LCM

FOLDING CARTONFOLDING CARTON

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11559-754-012019-10-21C16284748780-1956f9ecf-d42b-621f-e053-dbdaa90a74ada2f6c7d9-25b2-4187-8d2e-7c381007f6f0

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11559-754-01DAYWEAR PLUS MULTI PROTECTION TINTED MOISTURIZERSPF 151 in 1 CARTONCREAM11
11559-754-02DAYWEAR PLUS MULTI PROTECTION TINTED MOISTURIZERSPF 1550 mL in 1 TUBECREAM501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11559-754DAYWEAR PLUS MULTI PROTECTION TINTED MOISTURIZER SPF 15 (OCTINOXATE, OCTISALATE, AVOBENZONE) CREAM [ESTEE LAUDER INC]1Legacy NDC, 2 package rows20100413_a2f6c7d9-25b2-4187-8d2e-7c381007f6f0.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AVOBENZONEACTIVE INGREDIENTG63QQF2NOX1
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD511
OCTISALATEACTIVE INGREDIENT4X49Y0596W1
AVOBENZONEACTIVE MOIETYG63QQF2NOX1
OCTINOXATEACTIVE MOIETY4Y5P7MUD511
OCTISALATEACTIVE MOIETY4X49Y0596W1

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
11559-75411559-754-02, 11559-754-01

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
OCTINOXATE4Y5P7MUD51ACTIB
OCTISALATE4X49Y0596WACTIB
AVOBENZONEG63QQF2NOXACTIB

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
292e7622-c056-4857-b37e-76ff2a5a86dfa2f6c7d9-25b2-4187-8d2e-7c381007f6f02010-04-12WarningsExact identifier
spl id: 292e7622-c056-4857-b37e-76ff2a5a86df
spl set id: a2f6c7d9-25b2-4187-8d2e-7c381007f6f0

Reported adverse events (FAERS/openFDA)#

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