LidoSpra
LidoSpra is an FDA drug label for the active ingredient LIDOSPRA 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
- LIDOSPRA
- Manufacturer
- Oncora Pharma, LLC
- Product type
- HUMAN PRESCRIPTION DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 85477-325
- Application
- N/A
- Label effective
- 20260825
About this product
LidoSpra is an FDA-registered drug product whose active ingredient is LIDOSPRA. It is labelled by Oncora Pharma, LLC taken by topical and marketed as a human prescription drug product. Identifiers on file: NDC 85477-325, 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 LIDOSPRA are most often described in connection with: usage lidospra, topical analgesia, temporary relief, itching associated, minor burns, cuts scrapes, insect bites, skin irritations. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Indications & Usage
INDICATIONS AND USAGE LidoSpra™ is indicated for topical analgesia and for the temporary relief of pain and itching associated with minor burns, sunburn, minor cuts, scrapes, insect bites, minor skin irritations, and rashes due to poison ivy, poison oak, or poison sumac, or as directed by a healthcare provider.
Dosage & Administration
DOSAGE AND ADMINISTRATION Spray the affected area in sufficient quantity 2 to 4 times daily as needed or as directed by a healthcare provider.
Contraindications
CONTRAINDICATIONS LidoSpra™ is contraindicated in patients with known hypersensitivity to lidocaine or any component of the formulation.
Warnings
WARNINGS For external use only. Avoid contact with eyes. If irritation, sensitivity, or infection occurs, discontinue use. Keep out of reach of children.
Frequently asked questions
What is LidoSpra used for?
INDICATIONS AND USAGE LidoSpra™ is indicated for topical analgesia and for the temporary relief of pain and itching associated with minor burns, sunburn, minor cuts, scrapes, insect bites, minor skin irritations, and rashes due to poison ivy, poison oak, or poison sumac, or as directed by a healthcare provider.
Who makes LidoSpra?
Oncora Pharma, LLC is the labeler of record for LidoSpra.
What form does LidoSpra 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 LidoSpra prescription or over-the-counter?
The FDA label for this product is recorded as human prescription drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.
Has LidoSpra 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.