Active Ingredient
Benzocaine 6% w/v
Isopropyl alcohol 60% w/v
Medi-first Sting Relief Swab
FDA Label NDC 47682-234
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Unifirst First Aid Corporation for the product Medi-first Sting Relief (NDC 47682-234). 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, purpose, uses, 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 anesthetic
Antiseptic
Uses
For temporary relief of pain and itching associated with minor burns, scrapes and insect bites.
Warnings
For external use only.
Flammable, keep away from fire or flame.
Do Not Use
- in the eyes. If contact occurs, rinse thoroughly with water.
Stop Use And Ask A Doctor If
- irritation, redness or other symptoms develop
- 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
Adults and children 2 years of age and older: Apply to affected area 3-4 times daily.
Children under 2 years: CXonsult physician.
Other Information
- store at room temperature 59°-86°F (15°-30°C)
- tamper evident sealed packets
- do not use any opened or torn packets
Inactive Ingredients
purified water
Questions Or Comments?
1-800-634-7680
Medi-First Sting Relief Wipes Label
Medi-First®
Sting Relief Wipes
Benzocaine/ Isopropyl Acohol
Topical Anesthetic/ Antiseptic
Product # 23112
NET CONTENTS: 10 wipes per box
* Please review the disclaimer below.
