Hand Sanitizer
FDA Label NDC 62742-4185

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Allure Labs Inc for the product Hand Sanitizer (NDC 62742-4185). 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 - when using, 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.

Label Section Quick Index

Otc - Active Ingredient

Active Ingredients:

Ethyl Alcohol - 70%

Otc - Purpose

Purpose: Antimicrobial

Indications & Usage

Uses: To decrease the risk of skin infection in minor cuts, scrapes and burns.

Warnings

Warning: For External use only - Hands

Flammable: Keep away from heat and Flame

Otc - When Using

When using this products:

  • Keep out of eyes. In case of contact with eyes, flush thoroughly with water.

Otc - Stop Use

Stop use and ask a doctor if skin irritation develops. 

Otc - Keep Out Of Reach Of Children

Keep out of reach of children:

  • If product is swallowed, get medical help or contact a Poison Control Center right away.

Dosage & Administration

Directions:

  • Wet hands throughly with product and allow to dry without wiping. For children under 6, use only under adult supervision. Not recommended for infants.

Inactive Ingredient

Inactive Ingredients: Water (Aqua), Glycerin, Acrylate Copolymer, Sodium Hydroxide

Package Label.Principal Display Panel

Manufactured By

Allure Labs, Inc.

Hayward, CA 94544

www.allurelabs.com

* Please review the disclaimer below.