Active Ingredient
Benzalkonium Chloride 0.13%
Genrx Hand Sanitizing Spray
FDA Label NDC 59088-315
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Puretek Corporation for the product Genrx Hand Sanitizing (NDC 59088-315). 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 on, when using this product, stop use and ask a doctor if, 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
Purpose
Antiseptic
Uses
■ a topical antiseptic that protects against germs
Warnings
For external use only
Do Not Use On
■ deep or puncture wounds ■ animal bites ■ serious burns
When Using This Product
■ do not get into eyes
Stop Use And Ask A Doctor If
■ Irritation and redness develop
■ condition persists for more than 72 hours
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
■ wet hands thoroughly with product
■ allow to dry without wiping
■ repeat as necessary
Other Information
■ protect from freezing ■ avoid excessive heat
Inactive Ingredients
Aloe barbadensis (Aloe vera) leaf juice, butylene glycol, disodium EDTA, glycerin, phenoxyethanol,
purified water, sodium hyaluronate.
Genrx Hand Sanitizing Spray (8 Oz Label)
Label (Label)
* Please review the disclaimer below.
