LidoSpra
Spray · Topical
Uses
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 and administration
Spray the affected area in sufficient quantity 2 to 4 times daily as needed or as directed by a healthcare provider.
Contraindications
LidoSpra™ is contraindicated in patients with known hypersensitivity to lidocaine or any component of the formulation.
Warnings
For external use only. Avoid contact with eyes. If irritation, sensitivity, or infection occurs, discontinue use. Keep out of reach of children.
Precautions
Use only as directed. Excessive application may result in increased systemic absorption of lidocaine.
Description
LidoSpra™ is a topical spray containing Lidocaine 4.12%.
How supplied
LidoSpra™ (Lidocaine 4.12%) is supplied as a topical spray in a 30 mL (1 fl oz) container. NDC 85477-325-29 Store at 20°C to 25°C (68°F to 77°F). [See USP Controlled Room Temperature.]
Label text from the FDA structured product label by Oncora Pharma, LLC (revised Aug 25, 2026). Long sections are shortened; the complete label is on DailyMed.
Active ingredients
- Lidocaine in 1 product
LidoSpra NDC products (1)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 85477-325 | Lidocaine 41.2 mg/mL Spray | Oncora Pharma, LLC | UNAPPROVED DRUG OTHER |
Frequently asked questions
What is LidoSpra used for?
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?
LidoSpra is listed by 1 labeler in the FDA NDC directory, including Oncora Pharma, LLC.