Prescribing information (package insert) - Lidomax
DESCRIPTION
Lidomax™ is a topical gel containing Lidocaine Hydrochloride 2%, a local anesthetic. It is intended for topical application to intact skin.
INDICATIONS AND USAGE
Lidomax™ is indicated for topical analgesia as directed by a healthcare provider.
WARNINGS
For external use only. Not for ophthalmic use. Avoid contact with eyes. Do not use if allergic to lidocaine or any components of the formulation. Keep out of reach of children.
DOSAGE AND ADMINISTRATION
Apply a thin layer to the affected area 3 to 4 times daily or as directed by a healthcare provider. For external use only.
HOW SUPPLIED
Lidomax™ (Lidocaine HCl 2%) is supplied as a clear topical gel in a 3 oz (85 g) tube. NDC 85477-304-07
About this document
Source: FDA drug labeling via NLM DailyMed
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Drug information for Lidomax
| Rx or OTC |
Prescription (Rx)?
- This drug is available only with a prescription from a licensed healthcare provider.
- Rx
|
| Drug class |
Amide Local Anesthetic, Antiarrhythmic |
| Active ingredient |
Lidocaine 20 mg/g
|
| Dosage form |
Gel |
| Route |
Topical |
| Marketing status |
not in the current FDA NDC Directory |
| Company (applicant) |
Oncora Pharma, LLC |
| FDA approval |
UNAPPROVED DRUG OTHERUnapproved drug
|
| Manufacturers |
1 labelers list this drug on DailyMed |
| Packages (NDC) |
| Package |
|
20 mg/g – 85 g in 1 bottle, pump
NDC 85477-304-07
|
|
Source: FDA drug labeling via NLM DailyMed, data as of November 7, 2026. FDA data (DailyMed, Orange Book, Drug Shortages, enforcement reports). Not a substitute for the advice of a doctor or pharmacist.
