Home NDC 59050-104 EVR Sting Relief Wipe
Product NDC 59050-104
11-digit product format 590500104
Labeler code 59050
Product ID 59050-104_2b584d09-916d-00f8-e063-6294a90adbcf
Type HUMAN OTC DRUG
Nonproprietary name Benzocaine, Isopropyl Alcohol
Dosage form PATCH
Route TOPICAL
Labeler Changzhou Maokang Medical Products Co., Ltd.
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-01-10
Substance BENZOCAINE; ISOPROPYL ALCOHOL
Active strength 60; 600 mg/mL; mg/mL
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 EVR Sting Relief Wipe
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZOCAINE 60 mg/mL ISOPROPYL ALCOHOL 600 mg/mL
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 ND2M416302 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 59050-104-01 EVR Sting Relief Wipe 4 mL in 1 POUCH PATCH 4 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59050-104 EVR STING RELIEF WIPE (BENZOCAINE, ISOPROPYL ALCOHOL) PATCH [CHANGZHOU MAOKANG MEDICAL PRODUCTS CO., LTD.] 1 Current NDC, 1 package rows 20250112_2b584d09-916c-00f8-e063-6294a90adbcf.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 101 of 115 · 2,286 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 59050-104-01 59050010401 4 mL in 1 POUCH (59050-104-01) 4 ml 2025-01-10 No No Current