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Lidothol Patch

Generic: lidocaine and menthol

Unverified·never
RxCUI
1249758
Route
TOPICAL
ICD-10 indication
R52.9

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About Lidothol Patch

Lidothol is a prescription-strength medicated patch designed to provide targeted relief for localized pain. It contains two main active ingredients, lidocaine and menthol, which work together to reduce discomfort in the applied area. Lidocaine functions as a local anesthetic that temporarily numbs the site by interfering with pain signals sent from the nerves to the brain. Menthol acts as a counter-irritant and topical analgesic, creating a cooling sensation that helps soothe underlying aches. This patch is primarily used for the temporary management of minor aches and pains involving the muscles and joints. Healthcare providers often prescribe it to treat conditions such as backaches, arthritis, muscle strains, sprains, and bruises. Because the medication is absorbed directly through the skin at the site of the pain, it offers localized treatment that may help some patients avoid the systemic side effects sometimes associated with oral pain medications.

Copay & patient assistance

Detailed copay and financial assistance information is not publicly available for this medication at this time. Please consult your pharmacist or the manufacturer's official patient support program for more details.

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Prescribing information

From the FDA-approved label for Lidothol Patch. Official source: DailyMed (NLM) · Label effective May 20, 2025

Indications and usage
Uses For the temporary relief of pain.
Dosage and administration
Directions Adults 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 12 hours
Warnings
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 heart surgery • any patch from a pouch that has been opened for 7 or more days • in large quantities, particularly over raw surfaces or blistered areas • if tamper-evident seal is torn, broken, or missing • more than 2 patches per day unless directed by a doctor • children under 18 years of age Ask a doctor before use if you have • allergies to topical products • high blood pressure, heart disease, or kidney disease When using this product • Avoid contact with eyes. If eye contact occurs, rinse thoroughly with water. • The risk of heart attack or stroke may increase if you use more than directed or for longer than directed. Stop use and ask doctor if condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days. If pregnant of breast-feeding, ask a health professional before use Do not use during last 3 months of pregnancy because it may cause problems in the unborn child or complications during delivery. Keep out of reach of children. If put in mouth, seek medical help or contact a Poison Control Center right away. Dispose if the used patches by folding sticky ends together.

Label text is reproduced as-is from the FDA-approved label. We do not paraphrase, summarize, or omit. Content above is for informational purposes only and is not medical advice. Always consult your prescribing clinician or pharmacist before making decisions about your medication.

Conditions we've indexed resources for

Click a condition to see copay cards, grants, and PA rules specific to it. For the full list of FDA-approved indications, see Prescribing information above.

Prior authorization & coverage

PayerPAStep therapyCopay tier

Medicare Part D

Related drugs

How this page is sourced

  • Drug identity verified against openFDA NDC Directory.
  • Label text (when shown) originates from NLM DailyMed.
  • Copay and assistance URLs verified periodically; if you hit a broken link, tell us.