Home NDC 59050-706-01 Sting Relief Pad
Product NDC 59050-706
Requested package NDC 59050-706-01
11-digit product format 590500706
Labeler code 59050
Product ID 59050-706_276a73c8-6190-4e27-e063-6394a90a7d6a
Type HUMAN OTC DRUG
Nonproprietary name BENZOCAINE, ISOPROPYL ALCOHOL
Dosage form LIQUID
Route TOPICAL
Labeler Changzhou Maokang Medical Products Co., Ltd
Application M017
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-05-30
Substance BENZOCAINE; ISOPROPYL ALCOHOL
Active strength 60; .6 mg/g; mL/g
Pharmacologic classes Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
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 Sting Relief Pad
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZOCAINE 60 mg/g ISOPROPYL ALCOHOL .6 mL/g
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 RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 895749 Internal RxNorm 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 59050-706-01 Sting Relief Pad 0.34 g in 1 POUCH LIQUID 0.34 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59050-706 STING RELIEF PAD (BENZOCAINE, ISOPROPYL ALCOHOL) LIQUID [CHANGZHOU MAOKANG MEDICAL PRODUCTS CO., LTD] 3 Current NDC, 1 package rows 20241122_1936c5f4-274b-8e49-e063-6394a90ac642.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 77 of 152 · 3,029 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 59050-706-01 59050070601 .34 g in 1 POUCH (59050-706-01) 2024-05-30 No No Current