FACE IT AURA COLOR CONTROL

Product NDC
51523-658
11-digit product format
515230658
Labeler code
51523
Product ID
51523-658_08112381-fc1d-1cf1-e054-00144ff8d46c
Type
HUMAN OTC DRUG
Nonproprietary name
octinoxate, titanium oxide 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
51523-658-152020-01-31C16284748780-19d75b9cf-d73f-f424-e053-dadaa90a57ceFace it Aura Color Control 32800658

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51523-658-15FACE IT AURA COLOR CONTROL328006581 in 1 CARTONCREAM11
51523-658-15FACE IT AURA COLOR CONTROL3280065820 g in 1 CONTAINERCREAM201

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51523-658FACE IT AURA COLOR CONTROL 32800658 (OCTINOXATE, TITANIUM OXIDE AND ZINC OXIDE) CREAM [THEFACESHOP CO., LTD.]1Legacy NDC, 2 package rows20150224_08112381-fc1c-1cf1-e054-00144ff8d46c.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
51523-658-15515230658151 in 1 CARTONHistorical