Active Ingredients
Benzocaine, 6%
SD alcohol, 60%
After Bite Wipe Insect Sting Relief
FDA Label NDC 90107-3623
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Adventure Ready Brands for the product After Bite Wipe Insect Sting Relief (NDC 90107-3623). 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, use, warnings, do not use, stop use and ask a doctor if, 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
Topical Analgesic
Antiseptic
Use
- temporarily relieves pain and itching due to minor stings and insect bites
- to help reduce bacteria on the skin
Warnings
For external use only.
Flammable, keep away from fire or flame.
Do Not Use
- over large areas of the body
- in the eyes
- on broken skin or deep puncture wounds
Stop Use And Ask A Doctor If
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
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- 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
Store at room temperature
Inactive Ingredient
Purified water
Package Label.Principal Display Panel
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