Active Ingredients
Ethyl Alcohol 60%
Alcohol Hand Sanitizer Liquid
FDA Label NDC 87660-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangdong Yanze Biotechnology Co., Ltd. for the product Alcohol Hand Sanitizer (NDC 87660-001). 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 ingredients, purpose, use, warnings, when using this product, stop use and ask doctor, 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
Antimicrobia
Use
Hand sanitizer to help reduce bacteria on the skin.
Warnings
Flammable.Keep away from fire when using.
For external use only.
When Using This Product
do not use near the eyes in case of contact, rinse eyes thoroughly with water.
Stop Use And Ask Doctor
if irritation or rash appears and lasts.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
• Place enough product in your palm to thoroughly spread on both hands and rub into the skin until dry.
• Children under 6 years of age should be supervised when using this product.
Other Information
• Store below 106°F (41°C)
• May discolor certain fabrics or surfaces
• Validity period after opening: 12 months
Inactive Ingredient
Water, Carbomer, Taraxacum Officinale (Dandelion) Rhizome/Root Extract, Flos Farfarae Extract, Aminomethyl Propanol.
87660-001-01
30ml (01)
* Please review the disclaimer below.
