Everlit Care Hand Sanitizer Gel
FDA Label NDC 83807-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Everlit Global Inc. for the product Everlit Care Hand Sanitizer (NDC 83807-001). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - keep out of reach of children, dosage & administration, storage and handling, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

Active ingredient

Ethyl Alcohol, 75% v/v

Otc - Purpose

Purpose  Antiseptic

Indications & Usage

Uses

Kill germs and bacteria on skin to help reducing risk of infections

Warnings

Warnings

For external use only.

Flammable, keep away from fire or flame.

Do not use

near the eyes, if happens, rinse thoroughly with water.

if you are allergic to any of the ingredients

Stop use and ask a doctor if

irritation, excessive redness

or rash develops.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Do not use in the eyes. If irritation or redness occurs, stop use.

Dosage & Administration

Directions 

Apply a dime sized amount to palm of hand. Rub santizer all over surface of hands and fingers. Allow hands to dry. Discard properly after use.

Storage And Handling

Other information

Store at room temperature

Inactive Ingredient

Inactive ingredients

water, glycerin, propylene glycol, acrylates/ C10-C30 alkyl acrylate crossploymer, aminomethyl propanol, fragrance, denatonium benzoate, tocopheryl acetate, aloe barbadensis leaf jiuce, maltodextrin

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