ACONITE

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: ACONITE
Generic name: ACONITUM NAPELLUS
Manufacturer: ENERGIQUE, INC.
Product type: HUMAN OTC DRUG
SPL set ID: e5f8aa8c-0764-49e8-a2b1-4b8291eef882
SPL ID: 04259ae1-7e7d-4018-9866-9b0f378b2cfc
Version: 4
Effective date: 2023-06-07
Source export date: 2026-09-28
Source partition: 13
Source file: https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:34:40

Harmonized routes table
Harmonized routes
ORAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 9 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		ACONITE	openfda.brand_name
generic name		ACONITUM NAPELLUS	openfda.generic_name
manufacturer name		ENERGIQUE, INC.	openfda.manufacturer_name
ndc	package	44911-0209-1	openfda.package_ndc
ndc	product	44911-0209	openfda.product_ndc
ndc11	package	44911020901	derived:openfda.package_ndc
spl id		04259ae1-7e7d-4018-9866-9b0f378b2cfc	id
spl set id		e5f8aa8c-0764-49e8-a2b1-4b8291eef882	set_id
unii		U0NQ8555JD	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

WARNINGS: If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Do not use if tamper evident seal is broken or missing. Store in a cool, dry place.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.