Sting Relief Prep Pad Solution
FDA Label NDC 73288-006

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Ningbo Tianbo First Aid Product Co., Ltd. for the product Sting Relief Prep Pad (NDC 73288-006). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - keep out of reach of children, dosage & administration, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

Active Ingredient: Benzocaine 10% w/v

Otc - Purpose

Purpose: Topical Anesthetic

Indications & Usage

Uses: For temporary relief of pain and itching associated with minor burns, scrapes, and insect bites

Warnings

Warnings:

For external use only

Do not use: In the eyes, on broken skin, deep puncture wounds. I f unusal redness, swelling, irritation, or other symptoms occur, consult a physician immediately. 

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

Flammable. Keep away from fire or flame. Avoid contact with eyes. If this happens, rinse thoroughly with water.

Dosage & Administration

Directions: Wipe injection site vigorously and discard

Inactive Ingredient

Inactive Ingredient:

Isopropyl Alcohol, Purified Water

Package Label.Principal Display Panel

Image Description (Label)

Image Description (Label)

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