Home NDC 44911-0209 ACONITE
Product NDC 44911-0209
11-digit product format 449110209
Labeler code 44911
Product ID 44911-0209_04259ae1-7e7d-4018-9866-9b0f378b2cfc
Type HUMAN OTC DRUG
Nonproprietary name Aconitum napellus
Dosage form LIQUID
Route ORAL
Labeler ENERGIQUE, INC.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2015-07-15
Substance ACONITUM NAPELLUS WHOLE
Active strength 200 [hp_C]/mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2020-06-10 20:45 UTC · source 2020-06-10 excluded product product 44911-0209 I Inactivated by FDA excluded / ndc_excluded.zip 9bebd1f3094a…5416666fcb17…2020-06-10 20:45 UTC · source 2020-06-10 excluded package package 44911-0209 44911-0209-1 I Inactivated by FDA excluded / ndc_excluded.zip 9bebd1f3094a…5416666fcb17…
Additional Listing Data#
Finished product Yes
Brand name base ACONITE
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACONITUM NAPELLUS WHOLE 200 [hp_C]/mL
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.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 44911-0209-1 ACONITE 30 mL in 1 BOTTLE, DROPPER LIQUID 30 4
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 44911-0209 ACONITE (ACONITUM NAPELLUS) LIQUID [ENERGIQUE, INC.] 4 Current NDC, Legacy NDC, 1 package rows 20230609_e5f8aa8c-0764-49e8-a2b1-4b8291eef882.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 44911-0209-1 44911020901 30 mL in 1 BOTTLE, DROPPER (44911-0209-1) 30 ml 2015-07-15 0000-00-00 No No Current