Otc - Active Ingredient
Active Ingredient: Benzocaine 10% w/v
Lights Sting Relief Prep Pad Solution
FDA Label NDC 61333-211
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Lights Medical Manufacture Co., Ltd. for the product Lights Sting Relief Prep Pad (NDC 61333-211). 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.
Label Section Quick Index
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
Purified Water, Isopropyl Alcohol
* Please review the disclaimer below.
