Active Ingredient
Ethanol 65%
Apol Hand Sanitizer
FDA Label NDC 80082-201
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ecosem Co., Ltd for the product Apol Hand Sanitizer (NDC 80082-201). 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, use, warnings, when using this product, stop use and ask a doctor if, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
Hand clean sanitizer to help reduce bacteria on skin
Warnings
Flammable. Keep away from fire or flame.
For external use only.
When Using This Product
do not use in or near the eyes, ears and mouth. In case of contact, rinse eyes thoroughly with water.
Stop Use And Ask A Doctor If
irritation or rash appears and last.
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 briskly until dry.
Children under 6 years of age should be supervised when using this product.
Other Information
Store between 15-30C(59-86F)
Avoid freezing and excessive heat above 40C(104F)
Inactive Ingredients
Water, Glycerin, Propylene glycol, Carbomer, Aloe Vera gel Triethanolamine, Cinnamomum Cassia Bark Extract, Camellia Sinensis Leaf Extract, Chamaecyparis Lawsoniana Wood Oil
* Please review the disclaimer below.
