Muscle Cramp Pain Reliever Tablet
Product Images NDC 43689-0022

View Photos of 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 Muscle Cramp Pain Reliever (NDC 43689-0022). 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

Muscle Cramp Pain Reliever Ctn (Mgni0028 Muscle Cramp Pain Reliever Ctn 9 16 19)

Muscle Cramp Pain Reliever Ctn (Mgni0028 Muscle Cramp Pain Reliever Ctn 9 16 19)
Magnilife Muscle Cramp Pain Reliever 125 dissolving tablets carton packaging. The label highlights non-habit forming relief for muscle pain, cramping, and stiffness in legs, feet, back, hips, and joints. The labeler is The Magni Company. The package emphasizes the homeopathic product's use without known drug interactions or side effects, with instructions for oral dissolve under the tongue.*
FDA Label Image

Muscle Cramp Pain Reliever Lbl (Mgni0028 Muscle Cramp Pain Reliever Lbl)

Muscle Cramp Pain Reliever Lbl (Mgni0028 Muscle Cramp Pain Reliever Lbl)
Muscle Cramp Pain Reliever by The Magni Company, a homeopathic oral tablet product sold as 125 dissolving tablets. The label highlights relief for muscle pain, cramping, and stiffness in legs, feet, back, and hips. Active ingredients include Causticum, Colocynthis, Cuprum Metallicum, Magnesia Phosphorica, Phytolacca Decandra, Rhus Tox, Stannum Metallicum, and Veratrum Album in various homeopathic potencies. Also includes drug facts, warnings, directions, and inactive ingredients.*

* 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.