Active Ingredient
Lidocaine HCl 4%
Walgreens Burn Gel
FDA Label NDC 0363-2020
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Walgreens for the product Walgreens Burn (NDC 0363-2020). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, keep out of reach of children, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Topical analgesic
Uses
Temporarily relieves pain and itching due to: minor burns, sunburn, minor cuts, scrapes, insect bites, minor skin irritations
Warnings
For external use only
Do Not Use
In large quantities, particularly over raw surfaces or blistered areas
When Using This Product
Do not get into eyes
Stop use and ask doctor if
condition gets worse
symptoms last for more than 7 days
symptoms clear up and occur again within a few days
Keep out of reach of children
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- adults and children 2 years and over: apply to affected area not more than 3 to 4 times daily
- children under 2 years: ask a doctor
Other Information
Store between 20 °C and 25 °C (68 °F and 77 °F)
Inactive Ingredients
Aloe barbadensis (aloe vera) leaf juice, caprylyl glycol, dimethyl isosorbide, glycerin, hydroxyethyl cellulose, phenoxyethanol, purified water, vitamin E
Principal Display Panel
Carton (Carton Final Listing)
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