OTC - ACTIVE INGREDIENT SECTION
Active Ingredient
Menthol 4%
Active Ingredient
Menthol 4%
Active Ingredient Purpose
Menthol 4% Topical Analgesic
Directions
Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 2 years of age: consult a doctor.
Warnings
■ For external use only.
■ Avoid contact with the eyes.
■ If condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a doctor.
■ Do not apply to wounds or damaged skin.
■ Do not bandage tightly.
Uses
■ For the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises, and sprains. ■ Provides cooling and warming pain relief.
Other Information
■ Keep away from direct sunlight or heat.
■ Store at room temperature 15°-30°C (59°-86°F).
■ This package is child-resistant. Keep out of reach of children.
■ In case of accidental overdose or ingestion, call a doctor or poison control center immediately.
■ Do not use this product if seal is broken or missing.
Inactive Ingredients
Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Allantoin, Aloe Barbadensis Leaf Juice, Arnica Montana Flower Extract, Boswellia Serrata Resin Extract, Butyrospermum Parkii (Shea) Butter, C13-14 Isoparaffin, Cannabis Sativa Seed Oil, Carbomer, Centella Asiatica Leaf Extract, Cinnamomum Camphora (Camphor) Bark Oil, 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, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Methyl Sulfonyl Methane (MSM), PEG-100 Stearate, Phenoxyethanol, Polyacrylamide, Polysorbate 20, Pyridoxine HCl, Sodium Benzoate, Tocopheryl Acetate, Triethanolamine, Water
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72654-013-00 | Lightning Pain Relief | 65 g in 1 BOTTLE, PLASTIC | CREAM | 65 | 1 | |
| 72654-013-01 | Lightning Pain Relief | 101 g in 1 BOTTLE, PLASTIC | CREAM | 101 | 1 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 72654-013 | 72654-013-00, 72654-013-01 |
Every source-derived ingredient row is available through these pages.
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Lightning Pain Relief | MENTHOL | Ebanel Laboratories, Inc | 36edbc3f-501c-c1ea-e063-6394a90af6af | 2025-06-06 | Warnings | 72654-013-01 72654-013-00 72654-013 72654001301 72654001300 36edbc3f-501d-c1ea-e063-6394a90af6af 36edbc3f-501c-c1ea-e063-6394a90af6af |
Adverse event summaries are temporarily unavailable. Other product information remains available.