Active Ingredients
Benzocaine 6% w/v
Isopropyl Alcohol 60% w/v
Sting Relief Wipe
FDA Label NDC 59050-101
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Changzhou Maokang Medical Products Co., Ltd for the product Sting Relief Wipe (NDC 59050-101). 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, indications & usage, warnings, do not use, stop use, 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 Anesthetic
Antiseptic
Indications & Usage
For temporary relief of pain and itching associated with minor burns, scrapes and insect bites.
Warnings
For External Use Only
CautionFlammable
Do Not Use
in the eyes. If contact occurs, rinse thoroughly with water
Stop Use
If irritation, redness or other symptoms develop. Consult a doctor if the condition persists or gets worse.
Keep Out Of Reach Of Children.
If swallowed get medical help or contact a Poison Control Center right away.
Directions
Apply to affected area 3-4 times daily. For adults and children 2 years of age and older. Children under 2 years, consult physician.
Inactive Ingredient
Purified water
Package Label.Principal Display Panel
Image Of Pouch Label (Srw)
* Please review the disclaimer below.
