Active Ingredient
Alcohol 62% v/v
Hand Sanitizer Liquid
FDA Label NDC 87660-101
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 Hand Sanitizer (NDC 87660-101). 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, warning, do not use, stop use and ask a 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
Antiseptic
Use
Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Warning
Flammable.
Keep away from fire and flames.
For external use only.
Do Not Use
it near eye area. In case of contact, rinse eye thoroughly with water.
Stop Use And Ask A 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 immediately.
Directions
Apply into hand and thoroughly spray on both hands, rub until dry. Supervise children under 6 years of age when using this product to avoid swallowing.
Other Information
Store between 15 -30'C (59 -86°F) Avoid freezing and excessive heat above 40'C (104°F)
Inactive Ingredients
Glycerin, Water, Fragrance
87660-101-01
01 (New Pack 1)
02 (New Pack 2)
03 (New Pack 3)
04 (New Pack 4)
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