FDA.reportPublic FDA data

After Bite Wipe

Manufacturer
Adventure Ready Brands
Effective date
2021-01-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:55:26

Label at a glance#

ProductAfter Bite Wipe
Active ingredientLIDOCAINE HYDROCHLORIDE, ALCOHOL
Label structure10 sections

Indications and uses

First aid to help prevent infrection in minor scrapes and temporary relief of itching and insect bites

Dosage and administration

Adults and Children 2 years and older: Apply to cleaned affected area not more than 3 times daily. Children under 2 years of age: consult a doctor.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 50.0%

Lidocaine HCl 2.0%

Purpose

OTC - PURPOSE SECTION

First Aid Antiseptic

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

First aid to help prevent infrection in minor scrapes and temporary relief of itching 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 eyes
  • over raw or blistered areas

Stop use and ask a doctor

OTC - STOP USE SECTION

if conditions worsen or 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 kep or contact Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and Children 2 years and older: Apply to cleaned affected area not more than 3 times daily.

Children under 2 years of age: consult a doctor.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

benzalkonium chloride, menthol, purified water

After Bite

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

After Bite

Afterbite.com

Fast Relief from Insect Bites.

Contents: 1 single-use, premoistened towelette

Net contents: 0.037fl.oz.

Manufactured for: Tender Corporation Littleton, NH 03561 USA

LabelLabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
90107-3621-02024-12-27C16284748780-1f386c64a-0312-0266-e053-dadaa90a7c1aAfter Bite Wipe
90107-3621-12024-12-27C16284748780-1f386c64a-0312-0266-e053-dadaa90a7c1aAfter Bite Wipe
90107-3621-02023-01-30C16284748780-1f386c64a-0312-0266-e053-dadaa90a7c1aAfter Bite Wipe
90107-3621-12023-01-30C16284748780-1f386c64a-0312-0266-e053-dadaa90a7c1aAfter Bite Wipe

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
90107-362190107-3621-0, 90107-3621-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
MENTHOLL7T10EIP3AIACT
LIDOCAINE HYDROCHLORIDEV13007Z41AACTIR
ALCOHOL3K9958V90MACTIB
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT
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
2a460ba7-5634-0b5c-e063-6394a90acaabb984a26b-b2b0-09a8-e053-2995a90a6f922024-12-27WarningsExact identifier
spl set id: b984a26b-b2b0-09a8-e053-2995a90a6f92

Reported adverse events (FAERS/openFDA)#

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