Home NDC 72839-343 Pain, Burn, and Itch Relief
Product NDC 72839-343
11-digit product format 728390343
Labeler code 72839
Product ID 72839-343_29a5d04c-286a-9659-e063-6294a90a30bc
Type HUMAN OTC DRUG
Nonproprietary name Benzocaine 20%, Menthol 0.5%
Dosage form SPRAY
Route TOPICAL
Labeler Derma Care Research Labs, LLC
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-01-30
Substance BENZOCAINE; MENTHOL
Active strength 20; .5 g/100g; g/100g
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
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 Pain, Burn, and Itch Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZOCAINE 20 g/100g MENTHOL .5 g/100g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination U3RSY48JW5 Internal UNII lookup L7T10EIP3A Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 199864 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72839-343-03 Pain, Burn, and Itch Relief 85 g in 1 CAN SPRAY 85 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72839-343 PAIN, BURN, AND ITCH RELIEF (BENZOCAINE 20%, MENTHOL 0.5%) SPRAY [DERMA CARE RESEARCH LABS, LLC] 2 Current NDC, 1 package rows 20241222_fd9fe09f-3ae9-c5f5-e053-6394a90ad691.zip
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 97 of 151 · 3,010 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 72839-343-03 72839034303 85 g in 1 CAN (72839-343-03) 85 g 2023-01-30 No No Current