Dosage And Administration
Directions
Place enough product on hands to cover all surfaces. Rub hands together until dry.
Hand Sanitizer
FDA Label NDC 78770-4000
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Gutierrez Razo Y Asociados, S.a. De C.v. for the product Hand Sanitizer (NDC 78770-4000). 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 dosage and administration, inactive ingredients, uses, keep away from children, purpose, warnings and precautions, warnings, active ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredients
Inactive ingredients Water (Aqua), Glycerin, Carbomer, Triethanolamine
Uses
Use[s]
Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Keep Away From Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Purpose
Purpose Antmicrobial
Warnings And Precautions
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Warnings
Warnings
For external use only. Flammable. Keep away from heat or flame
Active Ingredient
Active ingredient. Ethyl Alcohol 70% v/v
Ask A Docto
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition
Stop Use
Stop use and ask a doctor if irritation or rash occurs.
* Please review the disclaimer below.
