Active Ingredient
Ethyl Alcohol 70%
Pro1tek Hand Sanitizer Gel
FDA Label NDC 52232-107
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Priority Environmental Solutions Inc. for the product Pro1tek Hand Sanitizer Gel (NDC 52232-107). 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, do not use, stop use and ask a doctor., keep out of reach of children., when using this product, 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 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 Use
In children less than 2 months of age. On open skin wounds.
Stop Use And Ask A Doctor.
If irritation or rash occurs. These may be signs of a serious condition.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
When Using This Product
Keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Directions
Apply a small amount to palm. Bristly rub, covering hand with product until dry. Supervise children under 6 years of age when using this product to avoid swallowing.
Other Information
Store between 33 and 110 F.
Inactive Ingredients
Water/Eau/Agua, Glycerin, Polyethylene glycol, Isopropyl Myristate, Aloe Barbadensis Leaf Juice, Tocopheryl Acetate (vitamin E), Isopropyl Alcohol, Carbomer, Triisopropanolamine
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