Active Ingredient
Ethyl Alcohol 62%
Genuine Hand Sanitizer
FDA Label NDC 52124-0006
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Genuine First Aid Llc for the product Genuine Hand Sanitizer (NDC 52124-0006). 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, do not use, stop use and consult a doctor, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antimicrobial
Uses
For handwashing to decrease bacteria on the skin.
Warnings
For external use only.
Flammable
Do Not Use
in the eyes. In case of contact, rinse eyes thoroughly with water.
Stop Use And Consult A Doctor
if irritation and redness develop and persist for more than 72 hours
Directions
Empty contents into palm. Rub hands until gel dissipates. Recommended for repeated use.
Inactive Ingredients
Propylene glycol, carbomer, titanium dioxide, purified water
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Package Label.Principal Display Panel
Genuine Hand Sanitizer
Instant Gel
Antiseptic Handwash
with Vitamin E and Aloe
Kills 99.9 percent of germs
Without Water
Active Ingredient:
Ethyl Alcohol 62 percent
Net Wt 0.9g (1/32 oz)
Manufactured in China For
Genuine First Aid.
* Please review the disclaimer below.
