Sting Relief Pad Swab
FDA Label NDC 0924-5202

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Acme United Corporation for the product Sting Relief Pad (NDC 0924-5202). 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, keep out of the reach of children., directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredients

Benzocaine, 6%

Isopropyl alcohol 60% w/v

Purpose

Topical Analgesic

Antiseptic

Use

For the temporary relief of pain and itching associated with minor burns, scrapes and insect bites. First aid to help prevent infection in minor cuts, scrapes and burns.

Warnings

For external use only

Flammable, keep away from fire or flame

Do Not Use

  • in eyes, if contact occurs flush with water
  • over large areas of the body

Keep Out Of The Reach Of Children.

If swallowed get medical help or contact a poison control center right away.

Directions

  • for adults and children 2 years of age or older, apply to affected area not more than 3 to 4 times daily
  • Children under 2 years: consult ohysician

Other Information

Store at room temperature

Inactive Ingredients

purified water

Package Labeling:

Label2 (Label2)

Label2 (Label2)

* Please review the disclaimer below.