AN ADC WHITENING BB

Product NDC
69153-060
11-digit product format
691530060
Labeler code
69153
Product ID
69153-060_cd5c1ea8-b21c-4438-8056-fa8147417a35
Type
HUMAN OTC DRUG
Nonproprietary name
Titanium Dioxide
Dosage form
CREAM
Route
TOPICAL
Labeler
AN Co Ltd.
Application
part352
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2014-08-01
Marketing end
0000-00-00
Substance
TITANIUM DIOXIDE
Active strength
3 g/50g
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
69153-060-012020-01-31C16284748780-19d75b9cf-efdb-f424-e053-dadaa90a57ce309aa9e8-a118-474a-8f57-a4dcc999f9d6

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69153-060-01AN ADC WHITENING BB50 g in 1 CARTONCREAM501

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Titanium DioxideACTIVE INGREDIENT15FIX9V2JPAN ADC WHITENING BB (TITANIUM DIOXIDE) CREAM [AN CO LTD.]1
TITANIUM DIOXIDEACTIVE MOIETY15FIX9V2JPAN ADC WHITENING BB (TITANIUM DIOXIDE) CREAM [AN CO LTD.]1
Propylene GlycolINACTIVE INGREDIENT6DC9Q167V3AN ADC WHITENING BB (TITANIUM DIOXIDE) CREAM [AN CO LTD.]1
WaterINACTIVE INGREDIENT059QF0KO0RAN ADC WHITENING BB (TITANIUM DIOXIDE) CREAM [AN CO LTD.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69153-060AN ADC WHITENING BB (TITANIUM DIOXIDE) CREAM [AN CO LTD.]1Legacy NDC, 1 package rows20140929_309aa9e8-a118-474a-8f57-a4dcc999f9d6.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
69153-060-016915300600150 g in 1 CARTON50 gHistorical