Lights Instant Sting Relief Pad
FDA Label NDC 61333-214

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 Instant Sting Relief Pad (NDC 61333-214). 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, indications & usage, warnings, otc - stop use, otc - keep out of reach of children, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Benzocaine 6% w/v

SD Alcohol: 60% w/v

Purpose

Topical Anesthetic

Antiseptic

Indications & Usage

Uses: For temporary relief of pain and itching associated with minor burns, sunburns, minor cut, scrapes, insect bites, or minor skin irritations

Warnings

Warnings:

For external use only. Flammable, keep away from fire or flame. Avoid contact with eyes, if this happens, rinse throughly with water. DO NOT USE with electrocautery procedures.

Otc - Stop Use

Stop use and ask a doctor if

  • irritation or redness develops
  • if condition worsens or persists for more than 7 days, or clear up and occur again within a few days, consult a physician

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

Directions

For adults and children 2 yeas of age or older: Apply to affected area not more than 3-4 times daily

Children under 2 yeas of age: Consult a doctor before use

Other Information

Store at room temperature 15-30 C (59-86F). Avoid excessive heat.

Inactive Ingredient

Inactive Ingredient

Purified Water

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