3CE DUO COLOR FACE BLUSH RETRO DRIVE

Product NDC
60764-061
11-digit product format
607640061
Labeler code
60764
Product ID
60764-061_b8c9cea5-61eb-4f54-a014-5af0882c65c5
Type
HUMAN OTC DRUG
Nonproprietary name
Titanium Dioxide
Dosage form
POWDER
Route
TOPICAL
Labeler
Nanda Co., Ltd
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2016-08-20
Marketing end
0000-00-00
Substance
TITANIUM DIOXIDE
Active strength
0 g/5g
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60764-061-022020-01-31C16284748780-19d75b9d0-357d-f424-e053-dadaa90a57cea1356f98-d62a-4197-b82c-4b435e195093

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60764-061-013CE DUO COLOR FACE BLUSH RETRO DRIVE5 g in 1 CONTAINERPOWDER51
60764-061-023CE DUO COLOR FACE BLUSH RETRO DRIVE1 in 1 CARTONPOWDER11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60764-0613CE DUO COLOR FACE BLUSH RETRO DRIVE (TITANIUM DIOXIDE) POWDER [NANDA CO., LTD]1Legacy NDC, 2 package rows20161004_a1356f98-d62a-4197-b82c-4b435e195093.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
60764-061-01607640061015 g in 1 CONTAINER5 gHistorical
60764-061-02607640061021 in 1 CARTONHistorical