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Lidogel

Generic: Lidocaine HCl

Verified·Apr 23, 2026
Manufacturer
Taro Pharmaceuticals
NDC
59088-466
RxCUI
2562183
Route
TOPICAL
ICD-10 indication
L29.9

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About Lidogel

What is this medication? Lidogel is a topical anesthetic medication that contains lidocaine as its active ingredient. It is primarily used to provide temporary relief from pain, itching, or discomfort associated with minor skin irritations such as sunburn, insect bites, small cuts, and scrapes. By numbing the surface of the skin or mucous membranes, it helps manage localized distress effectively. In clinical settings, healthcare professionals often use this gel to numb specific areas before minor medical procedures. It is frequently applied to facilitate the comfortable insertion of instruments like catheters or tubes into the body. The medication works by temporarily blocking the pathway of pain signals along nerves, ensuring that the patient feels less sensation in the treated area.

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 Lidogel. Official source: DailyMed (NLM) · Label effective Jan 11, 2023

Indications and usage
INDICATIONS: For temporary relief of pain and itching associated with minor burns, sunburn, minor cuts, scrapes, insect bites, and minor skin irritation.
Dosage and administration
DOSAGE AND ADMINISTRATION: Apply a thin film to the affected area two or three times daily or as directed by a physician.
Contraindications
CONTRAINDICATIONS: Tuberculous or fungal lesions of skin vaccinia, varicella, and acute herpes simplex and in persons who have shown hypersensitivity to any of its components. Lidocaine is contraindicated in patients with a known history of hypersensitivity to local anesthetics of the amide type.
Warnings
WARNINGS: For external use only. Not for ophthalmic use. Keep out of reach of children.
Adverse reactions
ADVERSE REACTIONS: During or immediately after treatment, the skin at the site of treatment may develop erythema or edema or may be the locus of abnormal sensation.
Use in pregnancy
USE IN PREGNANCY Teratogenic Effects; Pregnancy Category B. Reproduction studies have been performed for Lidocaine in rats at doses up to 6.6 times the human dose and have revealed no evidence of harm to the fetus caused by Lidocaine. There are, however, no adequate and well-controlled studies in pregnant women. Animal reproduction studies are not always predictive of human response. General consideration should be given to this fact before administering Lidocaine to women of childbearing potential, especially during early pregnancy when maximum organogenesis takes place.

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

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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.