FDA.reportPublic FDA data

TINTED MOISTURIZER

Manufacturer
Bobbi Brown Professional Cosmetics 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
2010-04-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:24:21

Label at a glance#

ProductTINTED MOISTURIZER SPF 15
Active ingredientOCTINOXATE, TITANIUM DIOXIDE
Label structure3 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS: OCTINOXATE 7.50% [] TITANIUM DIOXIDE 3.00%

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:


BOBBI BROWN

SPF 15 TINTED MOISTURIZER


1.7 FL OZ/OZ LIQ/50 ML


BOBBI BROWN PROFESSIONAL COSMETICS
NY NY 10022
FOLDING CARTON
FOLDING CARTON


FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64141-743-012019-10-21C16284748780-1956f9ecf-c13b-621f-e053-dbdaa90a74adaac12f07-c4a8-41f5-9379-5572b2b211e2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64141-743-01TINTED MOISTURIZERSPF 151 in 1 CARTONLIQUID11
64141-743-02TINTED MOISTURIZERSPF 1550 mL in 1 TUBELIQUID501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64141-743TINTED MOISTURIZER SPF 15 (OCTINOXATE, TITANIUM DIOXIDE) LIQUID [BOBBI BROWN PROFESSIONAL COSMETICS INC.]1Legacy NDC, 2 package rows20100501_aac12f07-c4a8-41f5-9379-5572b2b211e2.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
64141-74364141-743-02, 64141-743-01

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
OCTINOXATE4Y5P7MUD51ACTIB
TITANIUM DIOXIDE15FIX9V2JPACTIB

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
36f8b37b-41d6-4ddc-8b45-d472e7d80853aac12f07-c4a8-41f5-9379-5572b2b211e22010-04-30WarningsExact identifier
spl id: 36f8b37b-41d6-4ddc-8b45-d472e7d80853
spl set id: aac12f07-c4a8-41f5-9379-5572b2b211e2

Reported adverse events (FAERS/openFDA)#

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