Polar Pure Hand Sanitizer
FDA Label NDC 80608-000

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by 11569635 Canada Inc for the product Polar Pure Hand Sanitizer (NDC 80608-000). 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 drug facts, active ingredients:, purpose:, use:, warnings:, when using this product, stop use and ask a doctor, 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

Drug Facts

Active Ingredients:

Ethyl alcohol 70% v/v

Purpose:

Antimicrobial

Use:

Hand sanitizer to help reduce bacteria on the skin that could cause disease.Recommended for repeated use.

Warnings:

Flammable, keep away from fire or flame. For external use only.

When Using This Product

do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop Use And Ask A Doctor

if irritation or rash appears and lasts.

Keep Out Of Reach Of Children,

if swallowed get medical help or contact a poison control center right away

Directions:

Place enough product in your palm to thoroughly cover your hands. Rub hands briskly until dry. Children under 6 years of age should be supervised when using this product.

Other Information:

Store below 43 C (110 F). May discolor certain fabrics or surfaces.

Inactive Ingredients:

Water (Aqua), Glycerin, Carbomer, Triethanolamine

* Please review the disclaimer below.