FDA.reportPublic FDA data

ACONITUM, RADIX

Product NDC
60512-6445
11-digit product format
605126445
Labeler code
60512
Product ID
60512-6445_8202e548-8750-4c6b-8ec6-d2183f613565
Type
HUMAN OTC DRUG
Nonproprietary name
ACONITUM, RADIX
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 NAPELLUS ROOT
Active strength
6 [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
60512-6445-12025-12-28C16284748780-19d75b9d1-0783-f424-e053-dadaa90a57cea06eebe7-2fa3-4fc2-bc7b-ebbb6945645c
60512-6445-12020-01-31C16284748780-19d75b9d1-0783-f424-e053-dadaa90a57cea06eebe7-2fa3-4fc2-bc7b-ebbb6945645c

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ACONITUM NAPELLUS ROOTACTIVE INGREDIENTKPD2N7348XACONITUM, RADIX PELLET [HOMEOLAB USA INC.]1
ACONITUM NAPELLUS ROOTACTIVE MOIETYKPD2N7348XACONITUM, RADIX PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GACONITUM, RADIX PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554ACONITUM, RADIX PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6445ACONITUM, RADIX PELLET [HOMEOLAB USA INC.]1Legacy NDC20131023_a06eebe7-2fa3-4fc2-bc7b-ebbb6945645c.zip