Label: LIDOPRO PATCH- lidocaine and menthol patch
- NDC Code(s): 68788-8630-1
- Packager: Preferred Pharmaceuticals Inc.
- This is a repackaged label.
- Source NDC Code(s): 53225-1123
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 12, 2024
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- Official Label (Printer Friendly)
- Drug Facts
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Active IngredientLidocaine 4%
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Purpose Topical Anesthetic
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Active IngredientMenthol 1%
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Purpose Topical Analgesic
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UsesFor the temporary relief of pain.
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Warnings For 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 ...
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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 ...
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Other information• some 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 - ...
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Inactive Ingredientsdihydroxyaluminum aminoacetate, glycerol, methylparaben, polysorbate 80, propylene glycol, sodium polyacrylate, tartaric acid, water
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Questions?877-985-8377 - Relabeled By: Preferred Pharmaceuticals Inc.
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INGREDIENTS AND APPEARANCEProduct Information