FDA.reportPublic FDA data

ARBUTINUM

Product NDC
60512-6188
11-digit product format
605126188
Labeler code
60512
Product ID
60512-6188_bb5abab6-718e-4296-ae4b-818f72839a62
Type
HUMAN OTC DRUG
Nonproprietary name
ARBUTINUM
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
ARBUTIN
Active strength
3 [hp_X]/1
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
60512-6188-12025-12-28C16284748780-19d75b9d0-b008-f424-e053-dadaa90a57ce4a9e1325-89ab-4038-b774-4fc1d8dd70cb
60512-6188-12020-01-31C16284748780-19d75b9d0-b008-f424-e053-dadaa90a57ce4a9e1325-89ab-4038-b774-4fc1d8dd70cb

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ARBUTINACTIVE INGREDIENTC5INA23HXFARBUTINUM PELLET [HOMEOLAB USA INC.]1
ARBUTINACTIVE MOIETYC5INA23HXFARBUTINUM PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GARBUTINUM PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554ARBUTINUM PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6188ARBUTINUM PELLET [HOMEOLAB USA INC.]1Legacy NDC20131030_4a9e1325-89ab-4038-b774-4fc1d8dd70cb.zip