FACE IT AQUA UV COLOR CONTROL

Product NDC
51523-790
11-digit product format
515230790
Labeler code
51523
Product ID
51523-790_0fd8c46a-b0c9-52b3-e054-00144ff8d46c
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
ZINC OXIDE; OCTINOXATE; TITANIUM DIOXIDE
Active strength
0 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
51523-790-252020-01-31C16284748780-19d75b9d0-de88-f424-e053-dadaa90a57ce0fd8c46a-b0c8-52b3-e054-00144ff8d46c

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51523-790-25FACE IT AQUA UV COLOR CONTROL328007901 in 1 CARTONCREAM11
51523-790-25FACE IT AQUA UV COLOR CONTROL3280079020 g in 1 CONTAINERCREAM201

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51523-790FACE IT AQUA UV COLOR CONTROL 32800790 (OCTINOXATE, TITANIUM DIOXIDE AND ZINC OXIDE) CREAM [THEFACESHOP CO., LTD.]1Legacy NDC, 2 package rows20150226_0fd8c46a-b0c8-52b3-e054-00144ff8d46c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
51523-790-25515230790251 in 1 CARTONHistorical