FACE TONE

Product NDC
51523-365
11-digit product format
515230365
Labeler code
51523
Product ID
51523-365_20087532-7d49-5393-e054-00144ff88e88
Type
HUMAN OTC DRUG
Nonproprietary name
octinoxate, titanium dioxide and zinc oxide cream
Dosage form
CREAM
Route
TOPICAL
Labeler
THEFACESHOP CO., LTD.
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2015-10-01
Marketing end
0000-00-00
Substance
OCTINOXATE; TITANIUM DIOXIDE; ZINC OXIDE
Active strength
2 g/35g; g/35g; g/35g
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
51523-365-172020-01-31C16284748780-19d75b9cf-f57b-f424-e053-dadaa90a57ceFACE TONE Sunscreen Controller SPF30 PA++ 34200365

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51523-365-17FACE TONEController SPF301 in 1 CARTONCREAM11
51523-365-17FACE TONEController SPF3035 g in 1 TUBECREAM351

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51523-365FACE TONE CONTROLLER SPF30 (OCTINOXATE, TITANIUM DIOXIDE AND ZINC OXIDE CREAM) CREAM [THEFACESHOP CO., LTD.]1Legacy NDC, 2 package rows20151001_20087532-7d4a-5393-e054-00144ff88e88.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
51523-365-17515230365171 in 1 CARTONHistorical