Aconite Liquid
Product Images NDC 44911-0209

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This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Aconite (NDC 44911-0209). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Energique, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

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FDA Label Image

Enrg0607 Aconite 200c 7 20 21

Enrg0607 Aconite 200c 7 20 21
This is a warning label and description for a homeopathic remedy called ACONITE 200C. It is recommended that if pregnant or breastfeeding, individuals should ask a healthcare professional before using the remedy. If overdosed, individuals should seek immediate medical help or contact a Poison Control Center. The remedy may temporarily relieve sudden onset of illness with intense pain based on traditional homeopathic practice, but it is not FDA evaluated. The active ingredient is 100% of Aconitum Napellus 200C, and the inactive ingredients are Demineralized water and 20% Ethanol. The suggested dosage for adults and children over 5 years of age is 10 drops orally, once daily or as directed by a healthcare professional. If symptoms persist for more than 7 days, individuals should consult their healthcare professional, and the remedy is not recommended for use in children under 12 years of age. The product should be stored in a cool, dry place and kept out of reach of children. If the tamper-evident seal is broken or missing, individuals should not use it. The product is distributed by Energique, Inc. at their address in Iowa.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.