FACE IT AQUA UV COLOR CONTROL

Product NDC
51523-772
11-digit product format
515230772
Labeler code
51523
Product ID
51523-772_0fdc17fb-ad8b-24b6-e054-00144ff88e88
Type
HUMAN OTC DRUG
Nonproprietary name
octinoxate, 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
OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE
Active strength
1 g/20g; g/20g; g/20g
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
51523-772-222020-01-31C16284748780-19d75b9d0-8776-f424-e053-dadaa90a57ce0fdc17fb-ad8a-24b6-e054-00144ff88e88

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51523-772-22FACE IT AQUA UV COLOR CONTROL328007721 in 1 CARTONCREAM11
51523-772-22FACE IT AQUA UV COLOR CONTROL3280077220 g in 1 CONTAINERCREAM201

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51523-772FACE IT AQUA UV COLOR CONTROL 32800772 (OCTINOXATE, TITANIUM DIOXIDE AND ZINC OXIDE) CREAM [THEFACESHOP CO., LTD.]1Legacy NDC, 2 package rows20150226_0fdc17fb-ad8a-24b6-e054-00144ff88e88.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
51523-772-22515230772221 in 1 CARTONHistorical