FDA.reportPublic FDA data

AILANTHUS GLANDULOSUS

Product NDC
60512-6467
11-digit product format
605126467
Labeler code
60512
Product ID
60512-6467_3172bd7a-5fce-463b-b78f-103cc7627c01
Type
HUMAN OTC DRUG
Nonproprietary name
AILANTHUS GLANDULOSUS
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
AILANTHUS ALTISSIMA FLOWERING TWIG
Active strength
1 [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
60512-6467-12025-12-29C16284748780-19d75b9d0-dba9-f424-e053-dadaa90a57ce410f8c9e-3d91-4725-86d6-6666eafa709a
60512-6467-12020-01-31C16284748780-19d75b9d0-dba9-f424-e053-dadaa90a57ce410f8c9e-3d91-4725-86d6-6666eafa709a

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
AILANTHUS ALTISSIMA FLOWERING TWIGACTIVE INGREDIENT8P29O5P7XUAILANTHUS GLANDULOSUS PELLET [HOMEOLAB USA INC.]1
AILANTHUS ALTISSIMA FLOWERING TWIGACTIVE MOIETY8P29O5P7XUAILANTHUS GLANDULOSUS PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GAILANTHUS GLANDULOSUS PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554AILANTHUS GLANDULOSUS PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6467AILANTHUS GLANDULOSUS PELLET [HOMEOLAB USA INC.]1Legacy NDC20131023_410f8c9e-3d91-4725-86d6-6666eafa709a.zip