FDA.reportPublic FDA data

BRIGHTENING SPOT TREATMENT CORRECTOR

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 | NIPPON SHIKIZAI INC
Effective date
2010-04-19
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:24:15

Label at a glance#

ProductBRIGHTENING SPOT TREATMENT CORRECTOR SPF 25
Active ingredientOCTINOXATE, TITANIUM DIOXIDE
Label structure4 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS: OCTINOXATE 7.0% [] TITANIUM DIOXIDE 0.98%

OTC - WHEN USING SECTION

USAGE: DAB A SMALL AMOUNT DIRECTLY ONTO SPOT WITH PRECISION APPLICATOR. BLEND INTO SKIN WITH A BRUSH.

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   

BRIGHTENING

SPOT

TREATMENT

CORRECTOR

SPF 25

0.16 OZ/ 4.5 ML


BOBBI BROWN PROFESSIONAL COSMETICS INC

600 MADISON AVE

NEW YORK, NY 10022

folding cartonfolding carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64141-003-012019-10-21C16284748780-1956f9ecf-cb9d-621f-e053-dbdaa90a74ad25092818-0aaa-482d-9c45-04bd4e8ddf2e

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64141-003-01BRIGHTENING SPOT TREATMENT CORRECTORSPF 251 in 1 CARTONCREAM11
64141-003-02BRIGHTENING SPOT TREATMENT CORRECTORSPF 254.5 mL in 1 TUBE, WITH APPLICATORCREAM4.51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64141-003BRIGHTENING SPOT TREATMENT CORRECTOR SPF 25 (OCTINOXATE, TITANIUM DIOXIDE) CREAM [BOBBI BROWN PROFESSIONAL COSMETICS INC]1Legacy NDC, 2 package rows20100419_25092818-0aaa-482d-9c45-04bd4e8ddf2e.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
64141-00364141-003-02, 64141-003-01

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
d115cd2a-4994-463b-8fe5-cb0887fee26a25092818-0aaa-482d-9c45-04bd4e8ddf2e2010-04-19WarningsExact identifier
spl id: d115cd2a-4994-463b-8fe5-cb0887fee26a
spl set id: 25092818-0aaa-482d-9c45-04bd4e8ddf2e

Reported adverse events (FAERS/openFDA)#

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