FACE IT SMART COLOR CONTROL

Product NDC
51523-661
11-digit product format
515230661
Labeler code
51523
Product ID
51523-661_0811c661-f0d2-312f-e054-00144ff8d46c
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
ZINC OXIDE; ENSULIZOLE; TITANIUM DIOXIDE
Active strength
3 g/30mL; g/30mL; g/30mL
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
51523-661-182020-01-31C16284748780-19d75b9cf-d745-f424-e053-dadaa90a57ceFace It Smart 32800661

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51523-661-18FACE IT SMART COLOR CONTROL3280066130 mL in 1 CONTAINERCREAM301
51523-661-18FACE IT SMART COLOR CONTROL328006611 in 1 CARTONCREAM11

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51523-661FACE IT SMART COLOR CONTROL 32800661 (ENSULIZOLE, TITANIUM DIOXIDE AND ZINC OXIDE) CREAM [THEFACESHOP CO., LTD.]1Legacy NDC, 2 package rows20150225_0811c661-f0d1-312f-e054-00144ff8d46c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
51523-661-185152306611830 mL in 1 CONTAINER30 mlHistorical