BRIGHTENING SPOT TREATMENT CORRECTOR

Product NDC
64141-003
11-digit product format
641410003
Labeler code
64141
Product ID
64141-003_d115cd2a-4994-463b-8fe5-cb0887fee26a
Type
HUMAN OTC DRUG
Nonproprietary name
OCTINOXATE, TITANIUM DIOXIDE
Dosage form
CREAM
Route
TOPICAL
Labeler
Bobbi Brown Professional Cosmetics Inc
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2009-03-01
Marketing end
0000-00-00
Substance
OCTINOXATE; TITANIUM DIOXIDE
Active strength
7 mL/100mL; mL/100mL
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

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 Socrata Ingredients#

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

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
64141-003-01641410003011 in 1 CARTONHistorical
64141-003-02641410003024.5 mL in 1 TUBE, WITH APPLICATOR4.5 mlHistorical