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

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
ACONITE	ACONITUM NAPELLUS	ENERGIQUE, INC.	e5f8aa8c-0764-49e8-a2b1-4b8291eef882	2023-06-07	Warnings	Exact identifier ndc (product): 44911-0209

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.

Identifier, FDA.report destination table
Identifier	FDA.report destination
e5f8aa8c-0764-49e8-a2b1-4b8291eef882	Available on FDA.report

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
44911-0209-1	2023-06-07	C162847	48780-1	9d75b9d0-9eec-f424-e053-dadaa90a57ce	DRUG FACTS:
44911-0209-1	2023-01-30	C162847	48780-1	9d75b9d0-9eec-f424-e053-dadaa90a57ce	DRUG FACTS:
44911-0209-1	2020-06-26	C162847	48780-1	9d75b9d0-9eec-f424-e053-dadaa90a57ce	DRUG FACTS:
44911-0209-1	2020-01-31	C162847	48780-1	9d75b9d0-9eec-f424-e053-dadaa90a57ce	DRUG FACTS:

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#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ACONITUM NAPELLUS	ACTIVE INGREDIENT	U0NQ8555JD	ACONITE (ACONITUM NAPELLUS) LIQUID [ENERGIQUE, INC.]	1
ACONITUM NAPELLUS	ACTIVE MOIETY	U0NQ8555JD	ACONITE (ACONITUM NAPELLUS) LIQUID [ENERGIQUE, INC.]	1
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	ACONITE (ACONITUM NAPELLUS) LIQUID [ENERGIQUE, INC.]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	ACONITE (ACONITUM NAPELLUS) LIQUID [ENERGIQUE, INC.]	1

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

UNII, Preferred term, Matched term table
UNII	Preferred term	Matched term
U0NQ8555JD	ACONITUM NAPELLUS	Aconitum napellus

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