Active Ingredient
Alcohol 62% (v/v)
Genrx Anti-bacterial Gel Liquid
FDA Label NDC 59088-299
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 Anti-bacterial Gel (NDC 59088-299). 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, when using this product, stop use and ask a doctor if, keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
Hand sanitizer to help reduce bacteria on the skin
Warnings
Flammable. Keep away from fire or flame.
When Using This Product
do not use in or near eyes. In case of contact, rinse eyes throughly with water
Stop Use And Ask A Doctor If
If irritation or rash appears and lasts.
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center
Directions
■ Dispense and rub onto hands until dry. Do not rinse off.
■ Children under 6 years of age should use this product under supervision.
Other Information
■ Do not store above 110°F (43°C)
Inactive Ingredients
Aloe Barbadensis (aloe vera) Leaf Juice, Aminomethyl Propanol, Butyrospermum Parkii (Shea) Butter, Carbomer, Glycerin, Isopropyl Myristate, Water (Aqua)
Genrx Hand Sanitizing Gel (24 Fl Oz)
Label (Label)
* Please review the disclaimer below.
