Active Ingredients
Menthol 4%
The following Structured Product Label (SPL) was submitted to the FDA by Clinical Resolution Laboratory, Inc. for the product Lightning Pain Relief (NDC 63742-013). 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 active ingredients, purpose, uses:, warnings, do not use this product if, when using this product, stop use and ask a doctor if, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Menthol 4%
Cooling Pain Relief
Temporary relief from minor aches and pains of sore muscles and joints associated with arthritis, backache, strains and sprains.
(For external use only)
Condition worsens, or if symptoms persist more than 7 days, or clear up and reoccur.
if swallowed, call your Poison Control Center at 1 (800) 222-1222.
Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Allantoin, Aloe Barbadensis Leaf Juice Extract, Arnica Montana Flower Extract, Boswellia Serrata Extract, Butyrospermum Parkii (Shea) Butter, C13-14 Isoparaffin, Camphor, Cannabis Sativa Seed Oil, Carbomer, Centella Asiatica Leaf Extract, Cholesterol, Dimethicone, Dimethyl Isosorbide Dipotassium Glycyrrhizate, Disodium EDTA, Emu Oil, Ethoxydiglycol, Eucalyptus Globulus Leaf Oil, Glycerin, Glyceryl Stearate, Helianthus Annuus (Sunflower) Seed Oil, Isopropyl Myristate, Laureth-7, Lavandula Angustifolia (Lavender) Oil, Lecithin, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Methyl Sulfonyl Methane (MSM), PEG-100 Stearate, Phenoxyethanol, Polyacrylamide, Polysorbate 20, Purified Water, Pyridoxine HCL (Vit. B6), SD Alcohol 40-B, Sodium Benzoate, Tocopheryl Acetate, Triethanolamine
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