FDA.reportPublic FDA data

After Bite Wipe Insect Sting Relief

Manufacturer
Tender Corporation
Effective date
2019-09-26
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:00:35

Label at a glance#

ProductAfter Bite Wipe Insect Sting Relief
Active ingredientBENZOCAINE, ALCOHOL
Label structure11 sections

Dosage and administration

adults and children 2 year of age and older: apply to affected area not more than 3 to 4 times daily. children under 2 years of age: consult a doctor

Storage and handling

Store at room temperature

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzocaine, 6%

SD alcohol, 60%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic
Antiseptic

Use

INDICATIONS & USAGE SECTION

temporarily relieves pain and itching due to minor stings and insect bites

Warnings

WARNINGS SECTION

For external use only.

Flammable, keep away from fire or flame.

Do not use

OTC - DO NOT USE SECTION

  • over large areas of the body
  • in the eyes
  • on broken skin or deep puncture wounds

Stop use and ask a doctor if

OTC - STOP USE SECTION

condition worsens or if symptoms persist for more than 7 days or clears up and occurs again within a few days.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • adults and children 2 year of age and older: apply to affected area not more than 3 to 4 times daily.
  • children under 2 years of age: consult a doctor

Other information

STORAGE AND HANDLING SECTION

Store at room temperature

Inactive Ingredient

INACTIVE INGREDIENT SECTION

Purified water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

After Bite Wipe Insect Sting Relief

1 single use wipes

Responsibly made in China for:

Tender Corporation

944 Industrial park Rd.

Littleton, NH

afterbite.com

After Bite Wipe ISRAfter Bite Wipe ISR

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
44224-0014-12021-01-29C16284748780-1ba0f9c33-5ba1-a910-e053-dadaa90a0b85After Bite Wipe Insect Sting Relief
44224-0014-22021-01-29C16284748780-1ba0f9c33-5ba1-a910-e053-dadaa90a0b85After Bite Wipe Insect Sting Relief

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44224-0014-1After Bite Wipe Insect Sting Relief1000 mg in 1 PACKAGESWAB10002
44224-0014-2After Bite Wipe Insect Sting Relief100 in 1 BOXSWAB1002
44224-0014-2After Bite Wipe Insect Sting Relief1000 mg in 1 PACKETSWAB10002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44224-0014AFTER BITE WIPE INSECT STING RELIEF (BENZOCAINE,ALCOHOL) SWAB [TENDER CORPORATION]2Legacy NDC, 3 package rows20190927_936359f4-1617-823a-e053-2a95a90ae295.zip

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
44224-001444224-0014-1, 44224-0014-2

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
WATER059QF0KO0RIACT
BENZOCAINEU3RSY48JW5ACTIB
ALCOHOL3K9958V90MACTIB

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
937774d1-e43d-6f01-e053-2a95a90afdfa936359f4-1617-823a-e053-2a95a90ae2952019-09-26WarningsExact identifier
spl id: 937774d1-e43d-6f01-e053-2a95a90afdfa
spl set id: 936359f4-1617-823a-e053-2a95a90ae295

Reported adverse events (FAERS/openFDA)#

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