Instant Hand Sanitizer
FDA Label NDC 63940-601

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Harmon Stores Inc for the product Instant Hand Sanitizer (NDC 63940-601). 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 active ingredient, purpose, uses, warnings, stop use and ask a doctor, keep out of reach of children, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Ethyl Alcohol 62%

Purpose

Antiseptic

Uses

Decreases bacteria on hands

Warnings

For external use only

Flammable. Keep away from fire or flame

Stop Use And Ask A Doctor

if rash or irritation develops and lasts

Keep Out Of Reach Of Children

If swallowed, get medical help or contact a Poison Control Center.

Directions

Apply onto hands and rub until dry

Inactive Ingredients

Water, Aloe barbadensis Leaf Juice, Glycerin, Propylene Glycol, Triethanolamine, Carbomer

Labeling

Label (Label)

Label (Label)

* Please review the disclaimer below.