Sting Relief Medicated Pad
FDA Label NDC 72059-001

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 Sirius Packing Products Co., Ltd. for the product Sting Relief Medicated Pad (NDC 72059-001). 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, use, directions, warnings, otc - keep out of reach of children, inactive ingredients, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Medicinal Ingredient:Benzocaine6%

Purpose

Topical Anesthetic

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. 

Warnings

FOR EXTERNAL USE ONLY.FLAMMABLE,Keep away from fire or flame.

Do not use in the eyes ,if contact occurs ,flush eyes with water.

other information sotre at room temperature 15 OC-30 OC(59-86 OF)

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN. if swallowed get medical help or contact a Poison Control Center right away.

Inactive Ingredients

isopropyl alcohol,purified water

* Please review the disclaimer below.