Viragel Hand Sanitizer
FDA Label NDC 80007-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Comercial Emana, S.a. De C.v. for the product Viragel Hand Sanitizer (NDC 80007-001). 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 drug facts, active ingredient:, purpose:, use:, warnings:, when using this product, stop use and ask a doctor, 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
Active Ingredient:
Ethyl Alcohol 70% v/v
Purpose:
Antimicrobial
Use:
Hand sanitizer to help reduce bacteria on the skin
Warnings:
Flammable, Keep away from fire or flame.
For external use only.
When Using This Product
avoid contact with eyes. In case of contact , rinse eyes thoroughly with water.
Stop Use And Ask A Doctor
if redness or irritation develops and 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 and allow to dry. Children under 6 years of age should be supervised when using this product.
Other Information:
Store below 110°F (43°C ) may discolor certain fabrics or surfaces
Inactive Ingredients:
Aqua, Carbomer, Triethanolamine, Alpha-Tocopherol
Package Labeling:
Bolttle (Bolttle)
* Please review the disclaimer below.
