Instant Hand Sanitizer
FDA Label NDC 53152-1004

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Aoss Medical Supply, Inc. for the product Instant Hand Sanitizer (NDC 53152-1004). 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 - ask doctor, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

Active ingredientsEthyl Alcohol 62%

Otc - Purpose

PurposeAntiseptic

Indications & Usage

UsesTo help reduce bacteria on the hands that can potentially cause disease.

Warnings

WarningFor External Use Only.Flammable, Keep away from fire or flame.

Otc - When Using

When using this productAvoid contact with eyes, if this occurs rinse thoroughly with water and contact a physician.

Otc - Ask Doctor

Ask a doctor before use if you haveDeep wounds, animal bites or serious burns.

Otc - Stop Use

Stop use and ask a doctor ifsignificant irritation or sensitization occurs.

Otc - Keep Out Of Reach Of Children

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

Dosage & Administration

DIRECTIONS:Apply a liberal amount to hands and rub hands thoroughly until dry. Do not rinse or wipe off gel.

Inactive Ingredient

INACTIVE INGREDIENTS:Deionized water, Aloe barbadenis, Leaf Juice, Glycerin,Propylene glycol, Carbomer, Aminomethyl Propanol, Fragrance

* Please review the disclaimer below.