Checked
Walgreens Burn Pad
burn pad · Walgreens Burn Pad is an amide local anesthetic (over-the-counter) containing burn pad, made by Walgreens.
- Type
- Over the counter
- Drug class
- Amide Local Anesthetic
- Route
- Topical
- Manufacturers
- 1
For temporary relief of pain and itching associated with sunburn, minor burns, minor skin irritation, minor cuts, minor scrapes, insect bites
FDA boxed warning
Boxed warning
Box Warning Section Do not use if individual wrapper has been opened or damaged
Drug facts
- Generic name
- burn pad
- Active ingredients
- Lidocaine
- Drug class
- Amide Local AnestheticAntiarrhythmic
- Dosage forms
- Patch
- Label holder
- Walgreens
- FDA application
- M017
- Label updated
- 03/17/2026
Purpose
Topical anesthetic
Uses
For temporary relief of pain and itching associated with sunburn, minor burns, minor skin irritation, minor cuts, minor scrapes, insect bites
Directions
Adults abnd children 2 years and older Clean the burn area with mild soap and water gently apply burn pad over the burn or wound apply to the affected area not more than 3 to 4 times daily
Warnings
For external use only When using this product avoid contact with the eyes
Stop use and ask a doctor
Stop use Stop use and ask a doctor if condition worsens or does not improve, symptoms persist for more than 7 days or clear up and occur again within a few days
Pregnancy or breastfeeding
If pregnant or breastfeeding ask a health professional before use
Keep out of reach of children
If swallowed, get medical help or contact a poison control center right away
Other information
Store at 15 degrees to 30 degrees C (59 degrees to 86 degrees F)
Inactive ingredients
1,3-propanediol aloe barbadensis (aloe) leaf juice caprylyl glycol chlorphenesin dimethyl isosorbide hydroxyethyl cellulose phenoxyethanol tocopheryl acetate (vitamin E) water
Forms and strengths
From the FDA NDC Directory · 1 product codes
| Dosage form | Strength | Route | NDCs |
|---|---|---|---|
| Patch | 4.1 g/100g | topical | 1 |
Manufacturers and labels
1 FDA label
- WalgreensShown hereM017 · Label 03/17/2026 · NDC 0363-2789Full 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
Walgreens Burn Pad: common questions
- What is Walgreens Burn Pad used for?
- For temporary relief of pain and itching associated with sunburn, minor burns, minor skin irritation, minor cuts, minor scrapes, insect bites
- Does Walgreens Burn Pad have a boxed warning?
- Yes. The FDA label carries a boxed warning. A boxed warning is the FDA's strongest warning for serious or life-threatening risks.
- Is Walgreens Burn Pad a prescription drug?
- No. Walgreens Burn Pad is sold over the counter (OTC) without a prescription.
- Are there other products with the same active ingredient as Walgreens Burn Pad?
- Yes. Other FDA-listed products with the same active ingredients include Pain Relief Patches, Burn Relief, LIDOCAINE PAIN RELIEF Gel-Patch, Lidocaine Numbing Cream.
Source: U.S. Food and Drug Administration, openFDA drug label (SPL) and NDC Directory · Last updated 03/17/2026 · Label text is shown as published by the manufacturer. Not medical advice