Collavera

Gel · Topical

Prescription (Rx) Amide Local Anesthetic Antiarrhythmic

Uses

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

Dosage and administration

For topical use only. Apply a thin layer to the affected area 3 to 4 times daily or as directed by a healthcare provider. Avoid contact with eyes and mucous membranes.

Warnings

For external use only. Not for ophthalmic use. Avoid contact with eyes. Excessive application may result in systemic absorption. Use only as directed. Keep out of reach of children.

Overdosage

Excessive topical application may increase systemic absorption of lidocaine and may result in central nervous system and cardiovascular effects. In the event of overdose, discontinue use and seek medical attention.

Description

Collavera™ contains Lidocaine Hydrochloride 20 mg/g (2%) in a topical gel base.

How supplied

Collavera™ (Lidocaine Hydrochloride 20 mg/g) is supplied as a clear topical gel in a 1 oz (28.33 g) tube. NDC 85477-305-07

Label text from the FDA structured product label by Oncora Pharma, LLC (revised Feb 27, 2026). Long sections are shortened; the complete label is on DailyMed.

Active ingredients

Collavera NDC products (1)

NDCStrength & formLabelerType
85477-305Lidocaine 20 mg/g
Gel
Oncora Pharma, LLCUNAPPROVED DRUG OTHER

Frequently asked questions

What is Collavera used for?

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

Who makes Collavera?

Collavera is listed by 1 labeler in the FDA NDC directory, including Oncora Pharma, LLC.