FDA.reportPublic FDA data

ACONITUM FEROX

Product NDC
60512-6442
11-digit product format
605126442
Labeler code
60512
Product ID
60512-6442_4c5cf727-c17e-48bb-903f-cee51f84df0e
Type
HUMAN OTC DRUG
Nonproprietary name
ACONITUM FEROX
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 FEROX ROOT
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
60512-6442-12025-12-30C16284748780-19d75b9d0-57bb-f424-e053-dadaa90a57ceb2df20c9-f3a5-4c60-990b-4bf4f506acbf
60512-6442-12020-01-31C16284748780-19d75b9d0-57bb-f424-e053-dadaa90a57ceb2df20c9-f3a5-4c60-990b-4bf4f506acbf

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ACONITUM FEROX ROOTACTIVE INGREDIENTI4G31A93ZRACONITUM FEROX PELLET [HOMEOLAB USA INC.]1
ACONITUM FEROX ROOTACTIVE MOIETYI4G31A93ZRACONITUM FEROX PELLET [HOMEOLAB USA INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GACONITUM FEROX PELLET [HOMEOLAB USA INC.]1
SUCROSEINACTIVE INGREDIENTC151H8M554ACONITUM FEROX PELLET [HOMEOLAB USA INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-6442ACONITUM FEROX PELLET [HOMEOLAB USA INC.]1Legacy NDC20131023_b2df20c9-f3a5-4c60-990b-4bf4f506acbf.zip