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After Bite Wipe

Dosage form: liquid
Ingredients: LIDOCAINE HYDROCHLORIDE 20mg in 1mL, ALCOHOL 0.5mL in 1mL
Labeler: Tender Corporation
NDC Code: 44224-3621

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

After Bite Wipe

Active Ingredients

Ethyl Alcohol 50.0%

Lidocaine HCl 2.0%

Purpose

First Aid Antiseptic

Topical Analgesic

Uses

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

Warnings

For external use only.

Flammable, keep away from fire or flame

Do Not Use
  • over large areas of the body
  • in eyes
  • over raw or blistered areas

Stop use and ask a doctor

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

If swallowed get medical kep or contact Poison Control Center right away

Directions

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

benzalkonium chloride, menthol, purified water

After Bite

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

AFTER BITE WIPE 
ethyl alcohol, lidocaine hcl liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:44224-3621
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
LIDOCAINE HYDROCHLORIDE (LIDOCAINE) LIDOCAINE HYDROCHLORIDE ANHYDROUS20 mg  in 1 mL
ALCOHOL (ALCOHOL) ALCOHOL0.5 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
MENTHOL 
BENZALKONIUM CHLORIDE 
WATER 
Packaging
#Item CodePackage Description
1NDC:44224-3621-01.1 mL in 1 POUCH
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34811/01/2016
Labeler - Tender Corporation (064437304)
Registrant - Tender Corporation (064437304)
Establishment
NameAddressID/FEIOperations
Tender Corporation064437304manufacture(44224-3621)

 
Tender Corporation

Medically reviewed on Nov 5, 2018

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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