Hand Sanitizer
FDA Label NDC 79875-000
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Inndea, S.a. De C.v. for the product Hand Sanitizer (NDC 79875-000). 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(s), purpose, use(s), warnings, do not use, when using this product, stop use and ask a doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient(S)
Ethyl Alcohol 70% v/v
Purpose
Antiseptic
Use(S)
Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Warnings
For external use only. Flammable. Keep away from heat or flame. Do not mix use with other household chemicals.
Do Not Use
- In children less than two months of age.
- On open skin wounds.
When Using This Product
keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop Use And Ask A Doctor
if irritation or rash occurs. These maybe signs of serious condititon.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a poision control center right away.
Directions
- Place enough product on hands to cover all surfaces. Rub hands together until dry.
- Supervise children under 6 years age when using this product to avoid swallowing.
Other Information
- Store between 15-30C (59-86F)
- Avoid freezing and excesive heat above 40C (104F)
Inactive Ingredients
Purified water, glicerin, aloe vera extract, tocopheryl acetate (vitamin E).
Questions
+52 1 55 3775 1431 8:00 AM - 5:00 PM (EAST)
Package Labeling:10Ml
Bottle (Bottle)
* Please review the disclaimer below.
