Relaxing Legs Liquid
Product Images NDC 43689-0021

2 FDA label images from The Magni Company · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Relaxing Legs (NDC 43689-0021). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by The Magni Company, 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

Mgni0031 Relaxing Legs Ctn 9 17 19

Mgni0031 Relaxing Legs Ctn 9 17 19
Magnilife Relaxing Legs homeopathic liquid product label from The Magni Company, NDC 43689-0021. The label highlights the product as a nighttime sleep aid and pain reliever for unpleasant sensations, difficulty falling asleep, restlessness, pain, and discomfort. It contains 125 dissolving tablets. The label also states it is non-habit forming, with no known drug interactions or side effects, and includes directions for use with warnings and inactive ingredients listed.*
FDA Label Image

Relaxing Legs Lbl (Mgni0031 Relaxing Legs Lbl)

Relaxing Legs Lbl (Mgni0031 Relaxing Legs Lbl)
Drug Facts panel for MagniLife Relaxing Legs homeopathic oral liquid tablets. Includes warnings about pregnancy, breastfeeding, and child safety. Directions advise adults and children over 12 to dissolve 2 tablets under the tongue 2 to 3 times daily or as directed by a physician. Lists inactive ingredients and storage instructions. Active ingredients are homeopathic components for restlessness, leg discomfort, pain, and sleeplessness. Purposes and uses for temporary relief of leg discomfort with sleep issues are detailed. The package contains 125 dissolving tablets.*

* 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.