Home NDC 56104-914 Burn Relief
Product NDC 56104-914
11-digit product format 561040914
Labeler code 56104
Product ID 56104-914_560c29d7-28ba-6410-e063-6394a90ab90f
Type HUMAN OTC DRUG
Nonproprietary name Lidocaine
Dosage form AEROSOL, SPRAY
Route TOPICAL
Labeler Premier Brands of America Inc.
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-07-17
Substance LIDOCAINE
Active strength 5 mg/g
Pharmacologic classes Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Burn Relief
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength LIDOCAINE 5 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 98PI200987 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1442274 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 109 of 151 · 3,020 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 56104-914-01 56104091401 127 g in 1 CAN (56104-914-01) 127 g 2026-07-18 No No Current