Magnilife Pain Relieving Foot Cream
FDA Label NDC 43689-0063
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by The Magni Group, Inc. for the product Magnilife Pain Relieving Foot (NDC 43689-0063). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding drug facts, active ingredients (in cream), purpose, uses, warnings, keep out of reach of children, do not use, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients (In Cream)
Apis mellifica 3X HPUS
Gnaphalium leontopodium 6X HPUS
Sulphur 1X HPUS
Purpose
Relieves foot pain
External analgesic
Uses
Temporarily relieves foot pain
Warnings
• For external use only • Avoid contact with eyes
Keep Out Of Reach Of Children
• If symptoms persist for more than 7 days or worsen, consult your physician
Do Not Use
• on open wounds cuts, damaged, or infected skin
Directions
• Generously apply and massage into all surfaces of the feet, heels, and toes twice daily • Apply to legs as needed
Other Information
• Most beneficial when applied after bathing, showering, or a foot soak • The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopeia of the United States • These statements are supported by the traditional homeopathic principles
Inactive Ingredients
Beeswax, Camphor, Canola Oil, Carbomer, Ceteth-20, Cetyl Alcohol, Citrus Aurantium Bergamia (Bergamont) Fruit Oil, Ethylhexyl Stearate, Eucalyptus Globulus Leaf Oil, Glyceryl Stearate, Imidazolidinyl Urea, Menthol, Methylparaben, Methyl Salicylate, PEG-100 Stearate, Propylene Glycol, Propylparaben, Steareth-10, Steareth-21, Stearic Acid, Tocopheryl Acetate (Vitamin E), Tromethamine, Water, Xanthan Gum
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