Hand Sanitizer
FDA Label NDC 22431-581

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Blue Cross Laboratories, Inc. for the product Hand Sanitizer (NDC 22431-581). 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, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, inactive ingredient, package label.principal display panel, 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       purpose

Ethyl Alcohol 62%       Antimicrobial        

Otc - Purpose

Kills over 99% of most common germs

Otc - Keep Out Of Reach Of Children

Keep out of reach of children

Indications & Usage

Keep out of eyes.In case of eye contact immediately flush eyes with water then contact physician.

Warnings

Warning: flammable. Keep away from flame. If swallowed, contact physician. For external use only. Do not store above 110 degrees farenheit.

Dosage & Administration

directions:

put a thumbnail size amount in your palm and rub your hands together briskly until dry

Children under 6 years of age should be supervised when using Hand Rx.

Inactive Ingredient

Inactive Ingredients: Water, Glycerin, Propylene Glycol, Carbomer

Package Label.Principal Display Panel

Hand Rx

Hand Sanitizer

Kills 99.99% of germs

8 Fl Oz. (236 ml)

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