Active Ingredients
Ethyl Alcohol 50.0%
Lidocaine HCl 2.0%
After Bite Wipe
FDA Label NDC 44224-3621
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Tender Corporation for the product After Bite Wipe (NDC 44224-3621). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredients, purpose, uses, warnings, do not use, stop use and ask a doctor, keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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
* Please review the disclaimer below.
