Active Ingredient
Ethyl Alcohol 15% v/v
Hand Sanitizer
FDA Label NDC 76860-004
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Taizhou Huangyuan Liweir Cosmetic Technology Ltd. for the product Hand Sanitizer (NDC 76860-004). 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, do not use, 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
Purpose
Antiseptic
Use
Hand Sanitizer to help reduce bacteria that potentially can caise 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
- on open skin wounds
- on children less than 2 years of age.
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 may be signs of a serious condition.
Keep Out Of Reach Of Children.
If swallowed, get medical help or call a Poison Control Center right away.
Directions
- Place enough product on hands to cover all surfaces. Rub hands together until dry.
- Supervise children under 6 years of age when using this product to avoid swallowing.
Water (Aqua), Thiethanol amine, Carbomer, Glycerin, Propylene glycol, Aloe barbadensis extract
Other Information
- Store between 15-30'C (59-86')
- Avoid freezing and excessive heat above 40'C(104'F)
Package Label.Principal Display Panel
Display Panel (Label)
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