AN ADC WHITENING ESSENCE

Product NDC
69153-040
11-digit product format
691530040
Labeler code
69153
Product ID
69153-040_5177928d-3c59-4b3d-b93a-66af8347b5f5
Type
HUMAN OTC DRUG
Nonproprietary name
OATMEAL
Dosage form
CREAM
Route
TOPICAL
Labeler
AN Co Ltd.
Application
part347
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2014-08-01
Marketing end
0000-00-00
Substance
OATMEAL
Active strength
0 g/55g
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69153-040-012020-01-31C16284748780-19d75b9d0-cb11-f424-e053-dadaa90a57ce8f530244-9b50-48d6-a1e1-08716ae7756d

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69153-040-01AN ADC WHITENING ESSENCE55 g in 1 CARTONCREAM551

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69153-040AN ADC WHITENING ESSENCE (OATMEAL) CREAM [AN CO LTD.]1Legacy NDC, 1 package rows20140929_8f530244-9b50-48d6-a1e1-08716ae7756d.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
69153-040-016915300400155 g in 1 CARTON55 gHistorical