FDA.reportPublic FDA data

ARUM TRIPHYLLUM

Product NDC
60512-6520
11-digit product format
605126520
Labeler code
60512
Product ID
60512-6520_9855c435-ac0e-4c89-a60c-622b74a0208d
Type
HUMAN OTC DRUG
Nonproprietary name
ARUM TRIPHYLLUM
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
ARISAEMA TRIPHYLLUM ROOT
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
60512-6520-12025-12-30C16284748780-19d75b9d0-5da9-f424-e053-dadaa90a57ce98e708aa-9785-4419-8a39-cafb643a49bb
60512-6520-12020-01-31C16284748780-19d75b9d0-5da9-f424-e053-dadaa90a57ce98e708aa-9785-4419-8a39-cafb643a49bb

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ARISAEMA TRIPHYLLUM ROOTACTIVE INGREDIENTDM64K844DMARUM TRIPHYLLUM PELLET [HOMEOLAB USA INC.]1
ARISAEMA TRIPHYLLUM ROOTACTIVE MOIETYDM64K844DMARUM TRIPHYLLUM PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GARUM TRIPHYLLUM PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554ARUM TRIPHYLLUM PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6520ARUM TRIPHYLLUM PELLET [HOMEOLAB USA INC.]1Legacy NDC20131030_98e708aa-9785-4419-8a39-cafb643a49bb.zip