Sting Relief Wipe

Manufacturer: Changzhou Maokang Medical Products Co., Ltd
Effective date: 2023-02-01
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:53:43

Label at a glance#

ProductSting Relief Wipe

Active ingredientISOPROPYL ALCOHOL, BENZOCAINE

Label structure7 sections

Dosage and administration

Apply to affected area 3-4 times daily. For adults and children 2 years of age and older. Children under 2 years, consult physician.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzocaine 6% w/v

Isopropyl Alcohol 60% w/v

Purpose

OTC - PURPOSE SECTION

Topical Anesthetic

Antiseptic

INDICATIONS & USAGE SECTION

For temporary relief of pain and itching associated with minor burns, scrapes and insect bites.

Warnings

WARNINGS SECTION

For External Use Only

CautionFlammable

Do not use

OTC - DO NOT USE SECTION

in the eyes. If contact occurs, rinse thoroughly with water

Stop Use

OTC - STOP USE SECTION

If irritation, redness or other symptoms develop. Consult a doctor if the condition persists or gets worse.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to affected area 3-4 times daily. For adults and children 2 years of age and older. Children under 2 years, consult physician.

Inactive ingredient

INACTIVE INGREDIENT SECTION

Purified water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image of pouch label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
895749	benzocaine 6 % / isopropyl alcohol 60 % Medicated Pad	PSN	1
895749	benzocaine 60 MG/ML / isopropyl alcohol 0.6 ML/ML Medicated Pad	SCD	1
895749	benzocaine 6 % / isopropyl alcohol 60 % Medicated Pad	SY	1
895749	benzocaine 6 % / isopropyl alcohol 60 % Topical Swab	SY	1

DailyMed Pharmacologic Classes#

Class, Version, Type table
Class	Version	Type	Effective
BENZOCAINE Pharmacologic Class Indexing	2	Indexing - Pharmacologic Class	20180813

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
59050-101-01	2025-01-30	C162847	48780-1	2cef2736-74b2-d83d-e063-dadaa90ab31f	Ever Ready First Aid Sting Relief Wipe

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
59050-101-01	Sting Relief Wipe	0.4 mL in 1 POUCH	SWAB	0.4		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
59050-101	STING RELIEF WIPE (BENZOCAINE AND ISOPROPYL ALCOHOL) SWAB [CHANGZHOU MAOKANG MEDICAL PRODUCTS CO., LTD]	1	1 package rows	20230203_f3ae2c8a-4f5d-c3c1-e053-2995a90ae6f3.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

Sting Relief Wipe
Benzocaine and Isopropyl Alcohol
WATER
ISOPROPYL ALCOHOL
BENZOCAINE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
59050-101	59050-101-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
ISOPROPYL ALCOHOL	ND2M416302	ACTIB
BENZOCAINE	U3RSY48JW5	ACTIB

Source Document#

Source XML

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
f3ae2c8a-4f5e-c3c1-e053-2995a90ae6f3			f3ae2c8a-4f5d-c3c1-e053-2995a90ae6f3	2023-02-01	Warnings	Exact identifier spl id: f3ae2c8a-4f5e-c3c1-e053-2995a90ae6f3 spl set id: f3ae2c8a-4f5d-c3c1-e053-2995a90ae6f3

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.