Active Ingredient
Lidocaine HCl
The following Structured Product Label (SPL) was submitted to the FDA by Publix Super Markets, Inc. for the product Burnrelief (NDC 56062-942). 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, use, warnings, stop use and ask a doctor if, keep out of reach of children, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Lidocaine HCl
External analgesic
for the temporary relief of pain and itching associated with
For external use only
condition worsens, or if symptoms persist for more than 7 days or clean up and occur again within a few days
If swallowed, get medical help or contact a Poison Control Center right away
water, propylene glycol, glycerin, Aloe barbadensis leaf juice, triethanolamine, isopropyl alcohol, polysorbate 80, carbomer, diazolidinyl urea, menthol, disodium EDTA, blue 1, yellow 5
DISTRIBUTED BY PUBLIX SUPER MARKETS, INC.,
3300 PUBLIX CORPORATE PARKWAY
LAKELAND, FL 33811
publix.com
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