Home NDC 57556-010 Aconitum napellus
Product NDC 57556-010
11-digit product format 575560010
Labeler code 57556
Product ID 57556-010_4093b43a-691c-57cf-e063-6294a90adedc
Type HUMAN OTC DRUG
Nonproprietary name Aconite
Dosage form PELLET
Route ORAL
Labeler Historical Remedies
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2021-07-06
Substance ACONITUM NAPELLUS
Active strength 12 [hp_X]/g
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Aconitum napellus
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACONITUM NAPELLUS 12 [hp_X]/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination U0NQ8555JD Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 57556-010-02 Aconitum napellus 14 g in 1 BOTTLE, GLASS PELLET 14 9
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 57556-010 ACONITUM NAPELLUS (ACONITE) PELLET [HISTORICAL REMEDIES] 8 Current NDC, Legacy NDC, 1 package rows 20241105_c67753ee-08d9-a2fc-e053-2995a90aab99.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 57556-010-02 57556001002 14 g in 1 BOTTLE, GLASS (57556-010-02) 14 g 2021-07-06 0000-00-00 No No Current