Home NDC 0363-2053 Walgreens Pain Burn Itch Relief
Product NDC 0363-2053
11-digit product format 003632053
Labeler code 0363
Product ID 0363-2053_28f114af-a7fb-549c-e063-6394a90abbc3
Type HUMAN OTC DRUG
Nonproprietary name Benzocaine 20%, Menthol 0.5%
Dosage form SPRAY
Route TOPICAL
Labeler Walgreens
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-05-05
Substance MENTHOL; BENZOCAINE
Active strength 5; 200 mg/g; mg/g
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 Walgreens Pain Burn Itch Relief
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MENTHOL 5 mg/g BENZOCAINE 200 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination L7T10EIP3A Internal UNII lookup U3RSY48JW5 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 0363-2053-02 Walgreens Pain Burn Itch Relief 78 g in 1 CAN SPRAY 78 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0363-2053 WALGREENS PAIN BURN ITCH RELIEF (BENZOCAINE 20%, MENTHOL 0.5%) SPRAY [WALGREENS] 3 Current NDC, Legacy NDC, 1 package rows 20241213_cc6e4b42-fdd8-6ff7-e053-2995a90a3d1d.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 76 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 Marketing end Sample Exclude flag Status 0363-2053-02 00363205302 78 g in 1 CAN (0363-2053-02) 78 g 2022-05-05 0000-00-00 No No Current