Sting Relief Pad

Manufacturer: Yangzhou Suxiang Medical Instrument Co., Ltd.
Effective date: 2024-03-05
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-06-01 00:09:27

Label at a glance#

ProductSting Relief Pad

Active ingredientBENZOCAINE, ISOPROPYL ALCOHOL

Label structure11 sections

Indications and uses

For prevention of infection in minor scrapes andtemporary relief of itching insect bites

Dosage and administration

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

Storage and handling

store at room temperature 15° - 30° C (59° - 86° F)

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Benocaine 6% lsopropyl Alcohol 70%

OTC - PURPOSE SECTION

Topical analgesic

antiseptic

USES

INDICATIONS & USAGE SECTION

For prevention of infection in minor scrapes andtemporary relief of itching insect bites

WARNINGS SECTION

For external use only.
Flammable, keep away from fire or flame.

OTC - DO NOT USE SECTION

with electrocautery procedures.
In the eyes. If contact occurs, flush eyes with water.

OTC - STOP USE SECTION

Stop Use lf irritation and redness develop. If condition continues,consult your health care practitioner.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed,get medical help or contacta Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to affected area 3 or 4 times daily.
For adults and children 2 years of age and older.

Children under 2 years:consult physician.

other Information

STORAGE AND HANDLING SECTION

store at room temperature 15° - 30° C (59° - 86° F)

INACTIVE INGREDIENT SECTION

purified water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sting Relief Pad

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
72766-012-01	2026-01-29	C162847	48780-1	1030e365-2753-111a-e063-dadaa90a10e2	Sting Relief Medicated Pad
72766-012-01	2024-03-02	C162847	48780-1	1030e365-2753-111a-e063-dadaa90a10e2	Sting Relief Medicated Pad
72766-012-01	2024-01-30	C162847	48780-1	1030e365-2753-111a-e063-dadaa90a10e2	Sting Relief Medicated Pad

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72766-012-01	Sting Relief Pad	1 in 1 PACKET	SWAB	1		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72766-012	STING RELIEF PAD (STING RELIEF) SWAB [YANGZHOU SUXIANG MEDICAL INSTRUMENT CO., LTD.]	3	Legacy NDC, 1 package rows	20240307_e5ffbc65-1bf3-76e8-e053-2a95a90a67d7.zip

Products#

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

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

Sting Relief Pad
Sting Relief
WATER
BENZOCAINE
ISOPROPYL ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
72766-012	72766-012-01

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
BENZOCAINE	U3RSY48JW5	ACTIB
ISOPROPYL ALCOHOL	ND2M416302	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
12f34628-ef8b-f173-e063-6294a90ab59d			e5ffbc65-1bf3-76e8-e053-2a95a90a67d7	2024-03-05	Warnings	Exact identifier spl id: 12f34628-ef8b-f173-e063-6294a90ab59d spl set id: e5ffbc65-1bf3-76e8-e053-2a95a90a67d7

Reported adverse events (FAERS/openFDA)#

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