Lidomar
Lidomar is an FDA drug label for the active ingredient LIDOMAR manufactured by Oncora Pharma, LLC administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260825.
- Generic name
- LIDOMAR
- Manufacturer
- Oncora Pharma, LLC
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 85477-326
- Application
- M017
- Label effective
- 20260825
About this product
Lidomar is an FDA-registered drug product whose active ingredient is LIDOMAR. It is labelled by Oncora Pharma, LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 85477-326, application M017, label effective 20260825. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.
What it is used for
Across FDA labelling, products containing LIDOMAR are most often described in connection with: rashes due, temporary relief, itching associated, minor burns, cuts scrapes, insect bites, skin irritations, poison ivy. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Use(s) For the temporary relief of pain and itching associated with: minor burns sunburn minor cuts scrapes insect bites minor skin irritations rashes due to poison ivy rashes due to poison oak rashes due to poison sumac
Dosage & Administration
Directions Apply to the affected area 3 to 4 times daily or as directed by a healthcare provider.
Warnings
Warnings For external use only. Do not use if you are allergic to lidocaine or any of the ingredients. Avoid contact with eyes. Keep out of reach of children. Keep out of reach of childen
Frequently asked questions
What is Lidomar used for?
Use(s) For the temporary relief of pain and itching associated with: minor burns sunburn minor cuts scrapes insect bites minor skin irritations rashes due to poison ivy rashes due to poison oak rashes due to poison sumac
Who makes Lidomar?
Oncora Pharma, LLC is the labeler of record for Lidomar.
What form does Lidomar come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is Lidomar prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.
Has Lidomar been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.
Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.