ACONITE 200 [hp_C]/mL

Aconitum napellus · LIQUID · ENERGIQUE, INC.

No Recall History

Plain English

ACONITE is a liquid containing aconitum napellus at 200 [hp_C]/mL, taken oral. Manufactured by ENERGIQUE, INC..

Key Facts

Brand Name: ACONITE
Generic Name: Aconitum napellus
NDC Code (Product): 44911-0209
Manufacturer: ENERGIQUE, INC.
Strength: 200 [hp_C]/mL
Dosage Form: LIQUID
Route: ORAL
Marketing Status
Marketing Start: 07/15/2015

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

completed suicide4 reports

diarrhoea4 reports

headache4 reports

muscle spasms4 reports

paraesthesia4 reports

tinnitus4 reports

decreased appetite3 reports

hypersensitivity3 reports

neuropathy peripheral3 reports

arthralgia2 reports

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

INDICATIONS: May temporarily relieve sudden onset of illness with intense pain.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Dosage & Administration

DIRECTIONS: Adults and children 5 to 10 drops orally, 1 time daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

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.

Frequently Asked Questions

What is ACONITE used for?

ACONITE contains Aconitum napellus. It is a liquid taken oral. Consult your doctor for specific uses.

Is ACONITE a controlled substance?

ACONITE is not classified as a controlled substance by the DEA.

What is the generic name for ACONITE?

The generic name for ACONITE is Aconitum napellus. There are 12 other brand versions of Aconitum napellus.

What is the NDC code for ACONITE 200 [hp_C]/mL?

The NDC (National Drug Code) for ACONITE 200 [hp_C]/mL is 44911-0209, listed by ENERGIQUE, INC..

Product NDC

44911-0209

Package NDC

44911-0209-1

Other Aconitum Brands

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Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)