Label: LIDOPRO PATCH (LIDOCAINE 4%, MENTHOL 1%)- lidocaine and menthol patch patch
- NDC Code(s): 80425-0506-1
- Packager: Advanced Rx of Tennessee, LLC
- This is a repackaged label.
- Source NDC Code(s): 83881-402
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated March 20, 2025
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- Official Label (Printer Friendly)
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Active ingredientLidocaine 4% Menthol 1%
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PurposeExternal Anesthetic - External Analgesic
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UsesFor the temporary relief of pain.
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WarningsFor external use only. Do not use - on the face or rashes, on wounds or damaged skin - in the eyes, mouth, or other mucous membranes - on genitals - with a heating pad - right before or after heart ...
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DirectionsAdults 18 years and older: clean and dry affected area - open pouch and remove one patch - remove protective film from patch - apply one patch to the affected area of pain and leave in place for 8 to ...
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Other informationSome individuals may not experience pain relief until several minutes or hours after applying the patch - avoid storing product in direct sunlight - protect product from excessive moisture - store at ...
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Inactive ingredientsCarboxymethylcellose sodium, Dihydroxyaluminum aminoacetate, Edetate sodium, Glycerin, Kaolin, Methyl parahydroxybenzoate, Partially neutralized Sodium polyacrylate, Polyacrylic acid, Polysorbate ...
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PACKAGE LABEL PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCEProduct Information