FDA.reportPublic FDA data

STING RELIEF MEDICATED PAD

Manufacturer
Nantong Furuida Packaging Products Co., Ltd.
Effective date
2021-05-24
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:40:30

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

44

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1043353benzocaine 6 % Medicated PadPSN3
1043353benzocaine 60 MG/ML Medicated PadSCD3
1043353benzocaine 6 % Medicated WipeSY3
1043353benzocaine 6 % Topical SwabSY3

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
BENZOCAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73118-004-012024-01-30C16284748780-1ba0f9c33-4f7f-a910-e053-dadaa90a0b8573118-004sting relief
73118-004-012021-05-24C16284748780-1ba0f9c33-4f7f-a910-e053-dadaa90a0b8573118-004sting relief
73118-004-012021-01-29C16284748780-1ba0f9c33-4f7f-a910-e053-dadaa90a0b8573118-004sting relief

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73118-004-01STING RELIEF MEDICATED PAD200 in 1 BOXSWAB2003
73118-004-01STING RELIEF MEDICATED PAD1 in 1 POUCHSWAB13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73118-004STING RELIEF MEDICATED PAD (BENZOCAINE) SWAB [NANTONG FURUIDA PACKAGING PRODUCTS CO., LTD.]3Legacy NDC, 2 package rows20210525_89dbede6-4283-2f8c-e053-2a95a90aa71f.zip

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73118-00473118-004-01

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
NameUNIIKind
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT
BENZOCAINEU3RSY48JW5ACTIB

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
c3142ddb-74dd-a7d1-e053-2a95a90a26f389dbede6-4283-2f8c-e053-2a95a90aa71f2021-05-24WarningsExact identifier
spl id: c3142ddb-74dd-a7d1-e053-2a95a90a26f3
spl set id: 89dbede6-4283-2f8c-e053-2a95a90aa71f

Reported adverse events (FAERS/openFDA)#

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