Lidocaineside effects
lidocaine 0.04 MG/MG / menthol 0.01 MG/MG Medicated Patch
Adverse reactions
The most common adverse reactions occur at the application site, including dermatitis, itching or scaling. These tend to be dose-‐limiting and diminish with time. Serious adverse experiences following the administration of Lidothol are similar in nature to those observed in other amide anesthetic-‐containing agents. These adverse experiences are, in general, dose-‐related and may result from high plasma levels caused by excessive dosage, rapid absorption, or may result from hypersensitivity, idiosyncrasy, or a diminished tolerance on the part of the patient. Serious adverse experiences are generally systemic in nature. During or immediately after treatment with Lidothol, the skin at the site of application may develop redness, blisters, bruising, burning sensation, depigmentation, dermatitis, or mild irritation. Allergic Reactions Allergic and anaphylactoid reactions associated with Lidocaine, although rare, can occur. They are characterized by angioedema, bronchospasm, dermatitis, dyspnea, hypersensitivity, laryngospasm, pruritus, shock, and urticaria. If they occur, consult your doctor.
Text above is quoted in full from the FDA-approved drug label published by openFDA, effective May 20, 2025. Matched to this product by RxNorm code. Cross-references to other sections of the full prescribing information have been removed, since they point to a document not shown here. Nothing else is changed: no sentence is shortened, reworded or summarised.
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.
Text above is quoted in full from the FDA-approved drug label published by openFDA, effective May 20, 2025. Matched to this product by RxNorm code. Cross-references to other sections of the full prescribing information have been removed, since they point to a document not shown here. Nothing else is changed: no sentence is shortened, reworded or summarised.
Contraindications
Lidothol is contraindicated in patients with a known history of sensitivity to local anesthetics of the amide type, or to any other component of the product.
Text above is quoted in full from the FDA-approved drug label published by openFDA, effective May 20, 2025. Matched to this product by RxNorm code. Cross-references to other sections of the full prescribing information have been removed, since they point to a document not shown here. Nothing else is changed: no sentence is shortened, reworded or summarised.
This page reproduces regulatory text for reference. It is not medical advice, and KenyRx is not a pharmacy or a prescriber. Talk to a doctor or pharmacist about whether a medicine is right for you.
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