FDA.reportPublic FDA data

BRIGHTENING POWDER

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 | NIHON KOLMAR
Effective date
2010-04-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:24:10

Label at a glance#

ProductBRIGHTENING POWDER COMPACT FOUNDATION SPF 20
Active ingredientTITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE
Label structure2 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS: TITANIUM DIOXIDE 18.60% [] OCTINOXATE 7.00% [] ZINC OXIDE 5.80%

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL:

BOBBI BROWN

BRIGHTENING POWDER COMPACT FOUNDATION

SPF 20

REFILL/RECHARGE

NT WT. .38 OZ/ 11 g


DISTR. BOBBI BROWN PROFESSIONAL COSMETICS

NY, NY 10022

E3L7

BOBBI BROWN.COM

FOLDING CARTON
FOLDING CARTON


FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64141-718-012019-10-21C16284748780-1956f9ecf-bda2-621f-e053-dbdaa90a74ad25c955a5-f529-466d-bffe-c96561bae062

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64141-718-01BRIGHTENING POWDER COMPACT FOUNDATION SPF 201 in 1 CARTONPOWDER12
64141-718-02BRIGHTENING POWDER COMPACT FOUNDATION SPF 2011 g in 1 JARPOWDER112

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64141-718BRIGHTENING POWDER (TITANIUM DIOXIDE, OCTINOXATE, ZINC OXIDE) POWDER [BOBBI BROWN PROFESSIONAL COSMETICS INC. ]2Legacy NDC, 2 package rows20100406_25c955a5-f529-466d-bffe-c96561bae062.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
OCTINOXATEACTIVE INGREDIENT4Y5P7MUD512
TITANIUM DIOXIDEACTIVE INGREDIENT15FIX9V2JP2
ZINC OXIDEACTIVE INGREDIENTSOI2LOH54Z2
OCTINOXATEACTIVE MOIETY4Y5P7MUD512
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JP2
ZINC OXIDEACTIVE MOIETYSOI2LOH54Z2

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
64141-71864141-718-02, 64141-718-01

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
TITANIUM DIOXIDE15FIX9V2JPACTIB
OCTINOXATE4Y5P7MUD51ACTIB
ZINC OXIDESOI2LOH54ZACTIB

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
e64f5ee1-520b-466b-8252-09ab4d0a059d25c955a5-f529-466d-bffe-c96561bae0622010-04-06Exact identifier
spl id: e64f5ee1-520b-466b-8252-09ab4d0a059d
spl set id: 25c955a5-f529-466d-bffe-c96561bae062

Reported adverse events (FAERS/openFDA)#

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