FDA.reportPublic FDA data

ACONITUM LYCOCTONUM

Product NDC
60512-6443
11-digit product format
605126443
Labeler code
60512
Product ID
60512-6443_54ea7052-a368-4ff3-b2d4-6132e440ea49
Type
HUMAN OTC DRUG
Nonproprietary name
ACONITUM LYCOCTONUM
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-11
Marketing end
0000-00-00
Substance
ACONITUM LYCOCTONUM
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
60512-6443-12025-12-29C16284748780-19d75b9d0-8455-f424-e053-dadaa90a57ce88e70329-28c4-48db-bd8c-be27c1e903e1
60512-6443-12020-01-31C16284748780-19d75b9d0-8455-f424-e053-dadaa90a57ce88e70329-28c4-48db-bd8c-be27c1e903e1

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ACONITUM LYCOCTONUMACTIVE INGREDIENTEX75Q30TX6ACONITUM LYCOCTONUM PELLET [HOMEOLAB USA INC.]1
ACONITUM LYCOCTONUMACTIVE MOIETYEX75Q30TX6ACONITUM LYCOCTONUM PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GACONITUM LYCOCTONUM PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554ACONITUM LYCOCTONUM PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6443ACONITUM LYCOCTONUM PELLET [HOMEOLAB USA INC.]1Legacy NDC20131023_88e70329-28c4-48db-bd8c-be27c1e903e1.zip