Aconitum napellus

Manufacturer: Historical Remedies | Newton Laboratories, Inc.
Effective date: 2025-10-07
Label type: HUMAN OTC DRUG LABEL
Version: 9
Source: full-release
Hydrated at: 2026-06-01 02:37:20

Label at a glance#

ProductAconitum napellus

Active ingredientACONITUM NAPELLUS

Label structure10 sections

Contacts and useful links#

PhoneLabel contact800-676-6654

Websitewww.historicalremedies.com

www.historicalremedies.com

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Formulated for susceptibility to colds.

DOSAGE & ADMINISTRATION SECTION

Directions: Adults4 pellets; Children(4-12 years) 2 pellets; Dissolve under the tongue. Take every half hour as needed, or 4 times a day.

OTC - ACTIVE INGREDIENT SECTION

1% Aconitum napellus 12x

OTC - PURPOSE SECTION

Formulated for susceptibility to colds.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Organic beet-derived sucrose; gluten-free, lactose-free, non-GMO

QUESTIONS SECTION

OTC - QUESTIONS SECTION

Distributed by Historical Remedies; 122 S Wabasha, Saint Paul, MN 55107; 800-676-6654

www.historicalremedies.com

WARNINGS SECTION

Warning: Consult a doctor if symptoms persist more than 3 days or worsen. If pregnant or nursing, ask a doctor before use. Keep out of reach of children. Do not use if tamper-evident band is missing or broken.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding,ask a doctor before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

PACKAGE LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package label

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

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

Aconitum napellus
Aconite
SUCROSE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
57556-010	57556-010-02

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SUCROSE	C151H8M554	IACT
ACONITUM NAPELLUS	U0NQ8555JD	ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
8	2024-10-31	full-release	2026-06-01 02:28:46

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.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Aconitum napellus	ACONITE	Historical Remedies	c67753ee-08d9-a2fc-e053-2995a90aab99	2025-10-07	Warnings	Exact identifier ndc (package): 57556-010-02 ndc (product): 57556-010 ndc11 (package): 57556001002 spl id: 4093b43a-691c-57cf-e063-6294a90adedc spl set id: c67753ee-08d9-a2fc-e053-2995a90aab99

Reported adverse events (FAERS/openFDA)#

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