FDA.reportPublic FDA data

ACONITUM NAPELLUS

Product NDC
60512-1001
11-digit product format
605121001
Labeler code
60512
Product ID
60512-1001_23bba047-914d-4d20-a1c5-66a54b2c8eed
Type
HUMAN OTC DRUG
Nonproprietary name
ACONITUM NAPELLUS
Dosage form
PELLET
Route
ORAL
Labeler
HOMEOLAB USA INC
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
1995-10-24
Marketing end
0000-00-00
Substance
ACONITUM NAPELLUS
Active strength
3 [hp_X]/1
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60512-1001-12025-12-29C16284748780-19d75b9d1-0a50-f424-e053-dadaa90a57ce1e919d6d-87e4-439c-a76e-bdf354c6c298
60512-1001-12020-01-31C16284748780-19d75b9d1-0a50-f424-e053-dadaa90a57ce1e919d6d-87e4-439c-a76e-bdf354c6c298

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ACONITUM NAPELLUSACTIVE INGREDIENTU0NQ8555JDACONITUM NAPELLUS PELLET [HOMEOLAB USA INC]1
ACONITUM NAPELLUSACTIVE MOIETYU0NQ8555JDACONITUM NAPELLUS PELLET [HOMEOLAB USA INC]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GACONITUM NAPELLUS PELLET [HOMEOLAB USA INC]1
SUCROSEINACTIVE INGREDIENTC151H8M554ACONITUM NAPELLUS PELLET [HOMEOLAB USA INC]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60512-1001ACONITUM NAPELLUS PELLET [HOMEOLAB USA INC]1Legacy NDC20111130_1e919d6d-87e4-439c-a76e-bdf354c6c298.zip