Sting Relief

Manufacturer
NANTONG STRIP MEDICAL SUPPLY CO.,LTD.
Effective date
2010-05-26
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:24:38

Label at a glance#

ProductSting Relief
Active ingredientBenzocaine, Alcohol
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. DO NOT USE IN EYES, broken skin, deep puncture wounds, or if unusual redness, swelling, irritation or other symptoms occur, consult a physician immediately

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Medicinal Ingredient:Benzocaine6%, NON MEDICINAL: SD Alcohol 60%.

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. DO NOT USE IN EYES, broken skin, deep puncture wounds, or if unusual redness, swelling, irritation or other symptoms occur, consult a physician immediately

Cautions

WARNINGS SECTION

FLAMMABLE.KEEP OUT OF REACH OF CHILDREN. FOR EXTERNAL USE ONLY. AVOID CONTACT WITH EYES: if this happens, rinse thoroughly with water.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

purified water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

sting pad
sting pad

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046313benzocaine 6 % / ethanol 60 % Medicated PadPSN2
1046313benzocaine 60 MG/ML / ethanol 0.6 ML/ML Medicated PadSCD2
1046313benzocaine 6 % / ethanol 60 % Topical SwabSY2

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
35617-395-012019-10-21C16284748780-1956f9ecf-c990-621f-e053-dbdaa90a74adDrug Fact

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
35617-395-01Sting Relief1 in 1 PACKETSWAB12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
35617-395STING RELIEF (BENZOCAINE,ALCOHOL) SWAB [NANTONG STRIP MEDICAL SUPPLY CO.,LTD.]2Legacy NDC, 1 package rows20100526_8302b2bf-eabe-4786-b7d3-9867bc4e1283.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AlcoholACTIVE INGREDIENT3K9958V90M2
BenzocaineACTIVE INGREDIENTU3RSY48JW52
AlcoholACTIVE MOIETY3K9958V90M2
BenzocaineACTIVE MOIETYU3RSY48JW52
WATERINACTIVE INGREDIENT059QF0KO0R2

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
35617-39535617-395-01

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
BenzocaineU3RSY48JW5ACTIB
Alcohol3K9958V90MACTIB
WATER059QF0KO0RIACT

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
25bb85a9-3735-41ce-b8d1-d161f0d39eaf8302b2bf-eabe-4786-b7d3-9867bc4e12832010-05-26WarningsExact identifier
spl id: 25bb85a9-3735-41ce-b8d1-d161f0d39eaf
spl set id: 8302b2bf-eabe-4786-b7d3-9867bc4e1283

Reported adverse events (FAERS/openFDA)#

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