FACE IT AURA COLOR CONTROL SPF30 (REFILL), 01 RADIANT BEIGE

Product NDC
51523-659
11-digit product format
515230659
Labeler code
51523
Product ID
51523-659_080ff250-52b6-0992-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
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
51523-659-162020-01-31C16284748780-19d75b9cf-d61c-f424-e053-dadaa90a57ceFACE IT AURA COLOR CONTROL SPF30, PA++(REFILL) 01 RADIANT BEIGE 32800659

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51523-659-16FACE IT AURA COLOR CONTROL SPF30 (REFILL), 01 RADIANT BEIGE3280065920 g in 1 CONTAINERCREAM201
51523-659-16FACE IT AURA COLOR CONTROL SPF30 (REFILL), 01 RADIANT BEIGE328006591 in 1 CARTONCREAM11

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51523-659FACE IT AURA COLOR CONTROL SPF30 (REFILL), 01 RADIANT BEIGE 32800659 (OCTINOXATE, TITANIUM DIOXIDE AND ZINC OXIDE CREAM) CREAM [THEFACESHOP CO., LTD.]1Legacy NDC, 2 package rows20150127_080ff250-52b5-0992-e054-00144ff88e88.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
51523-659-165152306591620 g in 1 CONTAINER20 gHistorical