FDA.reportPublic FDA data

AESCULUS GLABRA

Product NDC
60512-6448
11-digit product format
605126448
Labeler code
60512
Product ID
60512-6448_b0af0423-03b6-4618-9ce9-c149f221bba6
Type
HUMAN OTC DRUG
Nonproprietary name
AESCULUS GLABRA
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
AESCULUS GLABRA NUT
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
60512-6448-12025-12-30C16284748780-19d75b9d0-57d0-f424-e053-dadaa90a57cedc0ef440-1db7-45aa-92fb-e4c0d524523a
60512-6448-12020-01-31C16284748780-19d75b9d0-57d0-f424-e053-dadaa90a57cedc0ef440-1db7-45aa-92fb-e4c0d524523a

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
AESCULUS GLABRA NUTACTIVE INGREDIENTIHY79HC33CAESCULUS GLABRA PELLET [HOMEOLAB USA INC.]1
AESCULUS GLABRA NUTACTIVE MOIETYIHY79HC33CAESCULUS GLABRA PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GAESCULUS GLABRA PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554AESCULUS GLABRA PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6448AESCULUS GLABRA PELLET [HOMEOLAB USA INC.]1Legacy NDC20131023_dc0ef440-1db7-45aa-92fb-e4c0d524523a.zip