Aconite
Aconitum napellus · Liquid · Oral
Active ingredient
ACTIVE INGREDIENT: (in each drop): 100% of Aconitum Napellus 200C.
Purpose
INDICATIONS: May temporarily relieve sudden onset of illness with intense pain.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Uses
INDICATIONS: May temporarily relieve sudden onset of illness with intense pain.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
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.
Keep out of reach of children
KEEP OUT OF REACH OF CHILDREN: Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
Directions
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.
Inactive ingredients
INACTIVE INGREDIENTS: Demineralized water, 20% Ethanol.
Questions?
QUESTIONS: Dist. by Energique, Inc. 201 Apple Blvd Woodbine, IA 51579 800-869-8078
Label text from the FDA structured product label by ENERGIQUE, INC. (revised Jun 7, 2023). Long sections are shortened; the complete label is on DailyMed.
Active ingredients
- Aconitum Napellus Whole in 1 product
Aconite NDC products (1)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 44911-0209 | Aconitum Napellus Whole 200 [hp_C]/mL Liquid | ENERGIQUE, INC. | UNAPPROVED HOMEOPATHIC |
Frequently asked questions
What is Aconite used for?
INDICATIONS: May temporarily relieve sudden onset of illness with intense pain.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
Who makes Aconite?
Aconite is listed by 1 labeler in the FDA NDC directory, including ENERGIQUE, INC..