Label at a glance#

ProductSTING RELIEF MEDICATED PAD

Active ingredientBENZOCAINE

Label structure6 sections

Dosage and administration

Apply to affected area not more than 3 to 4 times daily. For adults and children 2 years of age and older. Children under 2 years: consult a physician.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Medicinal Ingredient:Benzocaine6%

PURPOSE

OTC - PURPOSE SECTION

Topical Anesthetic

Use

INDICATIONS & USAGE SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to affected area not more than 3 to 4 times daily. For adults and children 2 years of age and older. Children under 2 years: consult a physician.

Warnings

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.

other information sotre at room temperature 15 ^OC-30 ^OC(59-86 ^OF)

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.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

isopropyl alcohol,purified water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1

RxCUI, Display, Full name table
RxCUI	Display	Full name	Type	Form / route
1043353	benzocaine 60 MG/ML Medicated Pad	benzocaine 60 MG/ML Medicated Pad	SCD Active

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
72059-001-01	2020-01-31	C162847	48780-1	9d75b9cf-e55e-f424-e053-dadaa90a57ce	72059-001sting relief

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72059-001-01	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
72059-001	STING RELIEF MEDICATED PAD (BENZOCAINE) SWAB [NANTONG SIRIUS PACKING PRODUCTS CO., LTD.]	1	Legacy NDC, 1 package rows	20180201_6428123f-895f-bc9e-e053-2991aa0a4f7d.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
ALCOHOL
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
72059-001	72059-001-01

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
ALCOHOL	3K9958V90M	IACT
WATER	059QF0KO0R	IACT
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
6428123f-895e-bc9e-e053-2991aa0a4f7d			6428123f-895f-bc9e-e053-2991aa0a4f7d	2018-02-01	Warnings	Exact identifier spl id: 6428123f-895e-bc9e-e053-2991aa0a4f7d spl set id: 6428123f-895f-bc9e-e053-2991aa0a4f7d

Reported adverse events (FAERS/openFDA)#

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

STING RELIEF MEDICATED PAD