ACONITUM NAPELLUS

Product NDC
62106-7197
11-digit product format
621067197
Labeler code
62106
Product ID
62106-7197_ed11a36a-7af4-376b-e053-2995a90abe60
Type
HUMAN OTC DRUG
Nonproprietary name
Aconite
Dosage form
GRANULE
Route
ORAL
Labeler
Seroyal USA
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2015-01-21
Marketing end
0000-00-00
Substance
ACONITUM NAPELLUS
Active strength
3 [hp_X]/1
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct62106-7197DDiscontinued by firm2026-07-31
excluded packagepackage62106-719762106-7197-4DDiscontinued by firm2026-07-31

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ACONITUM NAPELLUSACTIVE INGREDIENTU0NQ8555JDACONITUM NAPELLUS (ACONITE) GRANULE [SEROYAL USA]5
ACONITUM NAPELLUSACTIVE MOIETYU0NQ8555JDACONITUM NAPELLUS (ACONITE) GRANULE [SEROYAL USA]5
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GACONITUM NAPELLUS (ACONITE) GRANULE [SEROYAL USA]5
SUCROSEINACTIVE INGREDIENTC151H8M554ACONITUM NAPELLUS (ACONITE) GRANULE [SEROYAL USA]5

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
62106-7197-46210671970410 TUBE in 1 CARTON (62106-7197-4) > 140 GRANULE in 1 TUBE10 tube2015-01-210000-00-00NoNoCurrent