After Bite Wipe Insect Sting Relief

Manufacturer: Adventure Ready Brands
Effective date: 2020-12-10
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 23:35:02

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
to help reduce bacteria on the skin

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 clear up and occur 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

Label

RxCUI, Display, Full name table
RxCUI	Display	Full name	Type	Form / route
1046313	benzocaine 60 MG/ML / ethanol 0.6 ML/ML Medicated Pad	benzocaine 60 MG/ML / ethanol 0.6 ML/ML Medicated Pad	SCD Active

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1046313	benzocaine 6 % / ethanol 60 % Medicated Pad	PSN	2
1046313	benzocaine 60 MG/ML / ethanol 0.6 ML/ML Medicated Pad	SCD	2
1046313	benzocaine 6 % / ethanol 60 % Topical Swab	SY	2

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
90107-3623-1	2022-01-28	C162847	48780-1	d6a99b39-66ed-a426-e053-dadaa90af4c2	After Bite Wipe Insect Sting Relief
90107-3623-2	2022-01-28	C162847	48780-1	d6a99b39-66ed-a426-e053-dadaa90af4c2	After Bite Wipe Insect Sting Relief

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
90107-3623-1	After Bite Wipe Insect Sting Relief	1000 mg in 1 PACKAGE	SWAB	1000	2
90107-3623-2	After Bite Wipe Insect Sting Relief	1000 mg in 1 PACKET	SWAB	1000	2
90107-3623-2	After Bite Wipe Insect Sting Relief	100 in 1 BOX	SWAB	100	2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
90107-3623	AFTER BITE WIPE INSECT STING RELIEF (BENZOCAINE,ALCOHOL) SWAB [ADVENTURE READY BRANDS]	2	Legacy NDC, 3 package rows	20201211_b6208a41-fe05-d231-e053-2995a90aedb9.zip

Products#

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

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

After Bite Wipe Insect Sting Relief
BENZOCAINE,ALCOHOL
WATER
BENZOCAINE
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
90107-3623	90107-3623-1, 90107-3623-2

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
Name	UNII	Kind
WATER	059QF0KO0R	IACT
BENZOCAINE	U3RSY48JW5	ACTIB
ALCOHOL	3K9958V90M	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
b620fc3d-badd-a58f-e053-2995a90ab28d			b6208a41-fe05-d231-e053-2995a90aedb9	2020-12-10	Warnings	Exact identifier spl id: b620fc3d-badd-a58f-e053-2995a90ab28d spl set id: b6208a41-fe05-d231-e053-2995a90aedb9

Reported adverse events (FAERS/openFDA)#

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