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Burn Relief
lidocaine · Burn Relief is an amide local anesthetic (over-the-counter) containing lidocaine, made by 5 manufacturers.
- Type
- Over the counter
- Drug class
- Amide Local Anesthetic
- Route
- Topical
- Manufacturers
- 5
for temporary relief of pain and itching associated with: sunburn minor cuts scrapes minor burns insect bites minor skin irritations
Drug facts
- Generic name
- lidocaine
- Active ingredients
- Lidocaine
- Drug class
- Amide Local AnestheticAntiarrhythmic
- Dosage forms
- Aerosol, spray
- Label holder
- Premier Brands of America Inc.
- FDA application
- M017
- Label updated
- 07/17/2026
Active ingredients
Lidocaine 0.5%
Purpose
External analgesic
Uses
For temporary relief of pain and itching associated with: sunburn minor cuts scrapes minor burns insect bites minor skin irritations
Directions
Adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily children under 2 years of age: do not use, consult a doctor to apply to face, spray in palm of hand and gently apply
Warnings
For external use only. Extremely Flammable: Keep away from fire, sparks, and heated surfaces. Contents under pressure. Do not puncture or incinerate. Do not store at temperature above 120°F. Do not use in large quantities, particularly over raw surfaces or blistered areas. When using this product avoid spraying in the eyes use only as directed intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal. Stop use and ask a doctor if condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Do not use
In large quantities, particularly over raw surfaces or blistered areas.
When using this product
Avoid spraying in the eyes use only as directed intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal.
Stop use and ask a doctor
Condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days
Keep out of reach of children
If swallowed, get medical help or contact a Poison Control Center right away.
Inactive ingredients
Water, butane, propane, propylene glycol, aloe barbadensis leaf juice, carbomer, diazolidinyl urea, disodium cocoamphodipropionate, disodium edta, glycerin, methylparaben, propylparaben, simethicone, tocopheryl acetate, triethanolamine.
Questions?
Call 1-866-964-0939
Forms and strengths
From the FDA NDC Directory · 5 product codes
| Dosage form | Strength | Route | NDCs |
|---|---|---|---|
| Aerosol, spray | .5 g/100g | topical | 1 |
| Aerosol, spray | .64 g/127g | topical | 2 |
| Aerosol, spray | 5 mg/g | topical | 1 |
| Aerosol, spray | 40 mg/g | topical | 1 |
What pharmacies pay
National Average Drug Acquisition Cost (NADAC), week of 10/21/2026
Pharmacies paid about $0.0282 per gram across 1 package code.
NADAC is a survey of what retail pharmacies pay to buy a drug. It is not the price you pay at the counter, which depends on your insurance and the pharmacy.
Side effect reports to FDA
FDA Adverse Event Reporting System (FAERS), 57,975 reports that list lidocaine, data through 07/30/2026
Anyone can report a problem to FDA, and a report does not mean the drug caused the problem. Reports can be duplicated or incomplete, and counts depend on how widely a drug is used. Do not stop or change a medicine because of this list. Talk to your doctor or pharmacist.
Most often reported reactions
- Drug ineffective4,341
- Off label use4,128
- Pain3,661
- Fatigue3,499
- Product adhesion issue3,452
- Nausea3,399
- Headache3,310
- Product quality issue3,206
- Sinusitis2,562
- Dyspnea2,402
To report a side effect, use FDA MedWatch.
Manufacturers and labels
5 FDA labels
- Premier Brands of America Inc.Shown hereM017 · Label 07/17/2026 · NDC 56104-914Full label
- AmerisourceBergen Drug CorporationM017 · Label 07/01/2026 · NDC 46122-555Full label
- CVS PharmacyM017 · Label 10/29/2025 · NDC 69842-236Full label
- CVS Pharmacy, Inc.M017 · Label 04/06/2026 · NDC 51316-501Full label
- WALMART INC.M017 · Label 05/18/2026 · NDC 79903-036Full label
Related recalls
FDA drug recalls that name this drug or its active ingredient
- Class IIDrugOngoing10/14/2026Lidocaine Ointment USP, 5% (Generic for Xylocaine), packaged in a 50 g jar, Rx only, Mfg: Taro...Preferred Pharmaceuticals, Inc. · Failed Content Uniformity Specifications
- Class IIDrugOngoing09/23/2026Lidocaine Ointment USP, 5%, Speermint Flavor, 50 g Jar, Rx only, Mfd. by: Taro Pharmaceuticals Inc....SUN PHARMA /TARO · Failed Content Uniformity Specifications. Out of Specification for...
- Class IIDrugOngoing07/29/2026Lidocaine HCl Injection, USP, 2%, 100 mg per 5 mL (20 mg per mL), 25 Single Dose Vials, 5 mL per vial, Rx...Fresenius Kabi USA, LLC · 3 products · Presence of Particulate Matter: Hair was found in products
- Class IIIDrugOngoing07/29/2026Lidolog Kit, Kit Contains: Lidocaine HCl Injection, USP, 2% (2mL) vial, 1 Dose, Single use Only, Rx Only...Asclemed USA Inc. · Labeling: Not Elsewhere Classified: The label wrap covers the...
- Class IIDrugOngoing07/08/2026Accucaine, Kit contains: Lidocaine HCl Injection USP, 1% (10 mg/mL), 5 mL single dose ampule, Rx Only...Asclemed USA Inc. · 2 products · Lack of Assurance of Sterility
Burn Relief: common questions
- What is Burn Relief used for?
- for temporary relief of pain and itching associated with: sunburn minor cuts scrapes minor burns insect bites minor skin irritations
- Is Burn Relief a prescription drug?
- No. Burn Relief is sold over the counter (OTC) without a prescription.
- Are there other products with the same active ingredient as Burn Relief?
- Yes. Other FDA-listed products with the same active ingredients include Pain Relief Patches, LIDOCAINE PAIN RELIEF Gel-Patch, Lidocaine Numbing Cream, Lidocaine 4% Patch.
- Who makes Burn Relief?
- 5 manufacturers list Burn Relief with the FDA, including Premier Brands of America Inc., AmerisourceBergen Drug Corporation, CVS Pharmacy.
Source: U.S. Food and Drug Administration, openFDA drug label (SPL) and NDC Directory · Last updated 07/17/2026 · Label text is shown as published by the manufacturer. Not medical advice