FACE IT BB (Natural Beige)

Product NDC
51523-379
11-digit product format
515230379
Labeler code
51523
Product ID
51523-379_07d7d0ff-6508-147c-e054-00144ff8d46c
Type
HUMAN OTC DRUG
Nonproprietary name
octinoxate, titanium oxide and zinc oxide cream
Dosage form
CREAM
Route
TOPICAL
Labeler
THEFACESHOP CO., LTD.
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2014-11-20
Marketing end
0000-00-00
Substance
ZINC OXIDE; OCTINOXATE; TITANIUM DIOXIDE
Active strength
3 g/50mL; g/50mL; g/50mL
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
51523-379-072020-01-31C16284748780-19d75b9d0-b176-f424-e053-dadaa90a57ceFace It (Natural Beige) 32800379

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51523-379-07FACE IT BB (Natural Beige)3280037950 mL in 1 TUBECREAM501
51523-379-07FACE IT BB (Natural Beige)328003791 in 1 CARTONCREAM11

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51523-379FACE IT BB (NATURAL BEIGE) 32800379 (OCTINOXATE, TITANIUM OXIDE AND ZINC OXIDE CREAM) CREAM [THEFACESHOP CO., LTD.]1Legacy NDC, 2 package rows20150218_07d7d0ff-6507-147c-e054-00144ff8d46c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
51523-379-075152303790750 mL in 1 TUBE50 mlHistorical