Numyra™ 2.8% Gel

Manufacturer
Oncora Pharma, LLC
Effective date
2026-08-27
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-09-01 13:07:39

Label at a glance#

ProductNumyra
Active ingredientLIDOCAINE
Label structure8 sections

Indications and uses

Numyra™ is indicated for topical analgesia as directed by a healthcare provider.

Dosage and administration

For topical use only. Apply to the affected area 3 to 4 times daily or as directed by a healthcare provider.

Label contents#

Full prescribing information#

DESCRIPTION

DESCRIPTION SECTION

Numyra™ is a topical gel containing Lidocaine Hydrochloride 28 mg/g (2.8%).

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

Numyra™ is indicated for topical analgesia as directed by a healthcare provider.

CONTRAINDICATIONS

CONTRAINDICATIONS SECTION

Numyra™ is contraindicated in patients with known hypersensitivity to lidocaine or any component of the formulation.

WARNINGS

WARNINGS SECTION

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.

OVERDOSAGE

OVERDOSAGE SECTION

Excessive topical application may result in increased systemic absorption of lidocaine. In the event of overdose, discontinue use and seek medical attention.

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

For topical use only.

Apply to the affected area 3 to 4 times daily or as directed by a healthcare provider.

HOW SUPPLIED

HOW SUPPLIED SECTION

Numyra™ (Lidocaine Hydrochloride 28 mg/g) is supplied as a clear topical gel in a 3.5 oz (100 g) tube.

NDC 85477-0312-07

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

pdp
pdp

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130854770312074GTIN-13: 0854770312074
EAN-13: 0854770312074
GTIN-12: 854770312074
UPC-A: 854770312074
GTIN storage (14 digits): 00854770312074
numyra-1.jpg

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85477-31285477-312-07

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12026-08-25daily-update2026-08-27 00:02:26

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
NumyraNUMYRAOncora Pharma, LLC8707143f-dfd0-40b4-9594-9b2c569c32702026-08-27WarningsExact identifier
ndc (package): 85477-312-07
ndc (product): 85477-312
ndc11 (package): 85477031207
spl id: 6d953a59-a118-4535-a3cb-e71e6a531ffb
spl set id: 8707143f-dfd0-40b4-9594-9b2c569c3270

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.