Numyra
Numyra is an FDA drug label for the active ingredient NUMYRA 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 20260827.
- Generic name
- NUMYRA
- Manufacturer
- Oncora Pharma, LLC
- Product type
- HUMAN PRESCRIPTION DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 85477-312
- Application
- N/A
- Label effective
- 20260827
About this product
Numyra is an FDA-registered drug product whose active ingredient is NUMYRA. It is labelled by Oncora Pharma, LLC taken by topical and marketed as a human prescription drug product. Identifiers on file: NDC 85477-312, label effective 20260827. 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 NUMYRA are most often described in connection with: usage numyra, topical analgesia, directed healthcare. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Indications & Usage
INDICATIONS AND USAGE Numyra™ is indicated for topical analgesia as directed by a healthcare provider.
Dosage & Administration
DOSAGE AND ADMINISTRATION For topical use only. Apply to the affected area 3 to 4 times daily or as directed by a healthcare provider.
Contraindications
CONTRAINDICATIONS Numyra™ is contraindicated in patients with known hypersensitivity to lidocaine or any component of the formulation.
Warnings
WARNINGS For external use only. Not for ophthalmic use. Avoid contact with eyes. Excessive application may result in increased systemic absorption. Keep out of reach of children.
Frequently asked questions
What is Numyra used for?
INDICATIONS AND USAGE Numyra™ is indicated for topical analgesia as directed by a healthcare provider.
Who makes Numyra?
Oncora Pharma, LLC is the labeler of record for Numyra.
What form does Numyra 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 Numyra 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 Numyra 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.