Active Ingredient
Medicinal Ingredient:Benzocaine6%, NON MEDICINAL: SD Alcohol 60%.
Sting Relief
FDA Label NDC 35617-395
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Nantong Strip Medical Supply Co.,ltd. for the product Sting Relief (NDC 35617-395). 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 ingredient, use, directions, cautions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Use
For the temporary relief of pain and itching associated with minor burns,
scrapes and insect bites
Directions
Apply to affected area not more than 3 to 4 times daily. For adults and children
2 years of age and older. Children under 2 years: consult a physician. DO NOT
USE IN EYES, broken skin, deep puncture wounds, or if unusual redness, swelling,
irritation or other symptoms occur, consult a physician immediately
Cautions
FLAMMABLE.KEEP OUT OF REACH OF CHILDREN. FOR EXTERNAL USE ONLY. AVOID CONTACT
WITH EYES: if this happens, rinse thoroughly with water.
Inactive Ingredients
Purified water
* Please review the disclaimer below.
