FACE IT

Product NDC
51523-285
11-digit product format
515230285
Labeler code
51523
Product ID
51523-285_07d4e9a6-8732-5c4f-e054-00144ff88e88
Type
HUMAN OTC DRUG
Nonproprietary name
octinoxate, titanium oxide and zinc oxide cream
Dosage form
CREAM
Route
TOPICAL
Labeler
THEFACESHOP NORTH AMERICA, INC.
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2014-11-20
Marketing end
0000-00-00
Substance
OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE
Active strength
2 g/40mL; g/40mL; g/40mL
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
51523-285-032020-01-31C16284748780-19d75b9d0-5ad3-f424-e053-dadaa90a57ce07d4e9a6-8731-5c4f-e054-00144ff88e88

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51523-285-03FACE IT3280028540 mL in 1 TUBECREAM401
51523-285-03FACE IT328002851 in 1 CARTONCREAM11

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51523-285FACE IT 32800285 (OCTINOXATE, TITANIUM OXIDE AND ZINC OXIDE CREAM) CREAM [THEFACESHOP NORTH AMERICA, INC.]1Legacy NDC, 2 package rows20150225_07d4e9a6-8731-5c4f-e054-00144ff88e88.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
51523-285-035152302850340 mL in 1 TUBE40 mlHistorical