FACE IT SMART COLOR CONTROL

Product NDC
51523-677
11-digit product format
515230677
Labeler code
51523
Product ID
51523-677_0812c2b7-a915-3252-e054-00144ff88e88
Type
HUMAN OTC DRUG
Nonproprietary name
ensulizole, titanium dioxide and zinc oxide
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
ENSULIZOLE; TITANIUM DIOXIDE; ZINC OXIDE
Active strength
1 g/40g; g/40g; g/40g
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
51523-677-212020-01-31C16284748780-19d75b9d0-de8e-f424-e053-dadaa90a57ce0812c2b7-a914-3252-e054-00144ff88e88

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51523-677-21FACE IT SMART COLOR CONTROL3280067740 g in 1 CONTAINERCREAM401
51523-677-21FACE IT SMART COLOR CONTROL328006771 in 1 CARTONCREAM11

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51523-677FACE IT SMART COLOR CONTROL 32800677 (ENSULIZOLE, TITANIUM DIOXIDE AND ZINC OXIDE) CREAM [THEFACESHOP CO., LTD.]1Legacy NDC, 2 package rows20150226_0812c2b7-a914-3252-e054-00144ff88e88.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
51523-677-215152306772140 g in 1 CONTAINER40 gHistorical