Sting Relief Medicated Pad

Manufacturer: Davemed Healthcare Co., Ltd
Effective date: 2019-01-24
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:58:19

Label at a glance#

ProductSting Relief Medicated Pad

Active ingredientBENZOCAINE

Label structure9 sections

Indications and uses

First relief of pain and itching associated with minor burns, scrapes and insect bites

Dosage and administration

apply to affected area not more than 3 to 4 times daily for adults and children 2 years of age or older. children under 2 years, consult physician

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Benzocaine 6%

Purpose

OTC - PURPOSE SECTION

Purpose

Topical Anesthetic

Uses

INDICATIONS & USAGE SECTION

First relief of pain and itching associated with minor burns, scrapes and insect bites

WARNINGS SECTION

for external use only
flammable, keep away from fire or flame

Do not use

in the eyes
if contact occurs, flush eyes with water

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

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

apply to affected area not more than 3 to 4 times daily for adults and children 2 years of age or older.
children under 2 years, consult physician

Inactive ingredients

INACTIVE INGREDIENT SECTION

isopropyl alcohol, purified water

Other Information

OTHER SAFETY INFORMATION

Other Information

Store at room temperature 15 ^o - 30 ^oC (59 ^o - 86 ^oF)

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1043353	benzocaine 6 % Medicated Pad	PSN	1
1043353	benzocaine 60 MG/ML Medicated Pad	SCD	1
1043353	benzocaine 6 % Medicated Wipe	SY	1
1043353	benzocaine 6 % 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
70897-004-01	2024-01-30	C162847	48780-1	1030e365-5473-111a-e063-dadaa90a10e2	Sting relief medicated pad

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
70897-004-01	Sting Relief Medicated Pad	1 in 1 PACKET	SWAB	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
70897-004	STING RELIEF MEDICATED PAD (BENZOCAINE) SWAB [DAVEMED HEALTHCARE CO., LTD]	1	Legacy NDC, 1 package rows	20190125_80368076-8214-5b5a-e053-2991aa0ad16f.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

Sting Relief Medicated Pad
Benzocaine
WATER
ISOPROPYL ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
70897-004	70897-004-01

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
BENZOCAINE	U3RSY48JW5	ACTIB
WATER	059QF0KO0R	IACT
ISOPROPYL ALCOHOL	ND2M416302	IACT

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
80368076-8215-5b5a-e053-2991aa0ad16f			80368076-8214-5b5a-e053-2991aa0ad16f	2019-01-24	Warnings	Exact identifier spl id: 80368076-8215-5b5a-e053-2991aa0ad16f spl set id: 80368076-8214-5b5a-e053-2991aa0ad16f

Reported adverse events (FAERS/openFDA)#

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