Jointox Ai Liquid
Product Images NDC 44911-0586

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Jointox Ai (NDC 44911-0586). 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.

FDA Label Image

Jointox Ai (Enrg0570 Jointox Ai 4 15 21)

Drug information panel for Jointox AI homeopathic remedy by Energique, Inc. It includes warnings about pregnancy, breastfeeding, keeping out of reach of children, and overdose instructions. The label states indications for temporary relief of malaise, pain, swelling, and stiffness in small joints and big toes. Active ingredients are listed with 12.50% of various 30X homeopathic potencies, and inactive ingredients include demineralized water and 20% ethanol. Directions for use advise oral administration 3 times daily for adults and children over 5, with cautions for pediatric use and consultation if symptoms persist.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.