Cardioforce Liquid
Product Images NDC 43857-0437

Product Visual Gallery

This gallery contains 1 technical images submitted to the FDA as part of the official labeling for Cardioforce (NDC 43857-0437). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bioactive Nutritional, 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

Cardioforce Ii (Bani0110 Cardioforce Ii 2 22 17)

This is a warning label for a medication called Cardioforce I, which includes various active ingredients such as Abrotanum 3X and Boldo 3X. Pregnant or breast-feeding individuals should consult a medical professional before use, and the medicine should be kept away from children as an overdose could occur. Inactive ingredients include Demineralized Water, 25% Ethanol. It is indicated for temporary relief of mild dizziness, feeling faint, aching of legs, weakness of the lower limbs, sweling of legs. Users are directed to take 10 drops orally, three times a day, but should consult a physician for use in children under 12 years of age. The product is distributed by BioActive Nutritional, Inc. and comes in a 1 fl oz (30 ml) bottle.*

* 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.