Everlit Care Products Burn Relief Spray
FDA Label NDC 83807-032

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Everlit Global Inc. for the product Everlit Care Products Burn Relief (NDC 83807-032). 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 - do not use, otc - stop use, otc - keep out of reach of children, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

Active ingredient

Lidocaine HCI: 2%

Otc - Purpose

Purpose

Topical Pain Relief

Indications & Usage

Uses

Temporary pain relief associated with minor burns.

Warnings

Warnings

For external use only.

Otc - Do Not Use

Do not use

  • in the eyes
  • in large quantities, particularly over raw or blistered areas
  • if allergic to any ingredient
  • on deep puncture wounds or serious burns

Otc - Stop Use

Stop use and seek medical help

if the condition worsens or persist for more than 7 days or clears up and returns

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

Dosage & Administration

Directions

Spray and even layer of brun spray over cleaned affected area not more than 3 to 4 times daily

Chilrdren under 12 years of age: ask a doctor

Other Information

Store at room temperature

Inactive Ingredient

Inactive ingredients

Aminomethyl Propanol, Glycerin, Hydroxypropyl Methylcellulose,  Melaleuca Alterniflia (Tea Tree) Leaf Oil, Octoxyol 9, PEG-40 Hydrogenated Castor Oil, Phenoxyethanol, Polyethylene Glycol,  Water

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