Tego Systems Professional Grade Hand Sanitizer
FDA Label NDC 81497-700
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Tego Systems Corp for the product Tego Systems Professional Grade Hand Sanitizer (NDC 81497-700). 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, uses, warnings, 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
Active Ingredient
Ethyl alcohol 75%
Purpose
Antiseptic
Uses
Hand Sanitizer to help decrease bacteria on the skin
Warnings
External use only-hands
Flammable. Keep away from heat or flame.
When Using This Product
Keep out of eyes. In case of contact with eyes, flush thoroughly with water.
Stop Use And Ask A Doctor If
skin irritation develops.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison control Center right away.
Directions
- Put enough product in your palm to cover hands and rub hands together until dry.
- Children under 6, should be supervised when using this product.
Other Information
- Store below 110°F (43°C)
- May discolor some fabrics or surfaces
Inactive Ingredients
- Vitamin E, 1,2-Propanediol, carbomer, triethanolamine, water
Package Labeling:
Bottle (Bottle)
* Please review the disclaimer below.
