Active Ingredient(S)
ETHYL ALCOHOL 75%
Hand Sanitizer
FDA Label NDC 75541-015
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ningbo Meiteli Cosmetics Co., Ltd for the product Hand Sanitizer (NDC 75541-015). 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(s), purpose, use, warnings, do not use, otc - when using, otc - stop use, otc - 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
Use Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Warnings
Warnings For external use only. Flammable. Keep away from heat or flame.
Do Not Use
Do not use
●on open skin wounds.
●on children less than 2 years of age.
Otc - When Using
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes,ninse eyes thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if imitation or rash occurs. These may be signs of a serious condition.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
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.
Other Information
1.Store between 15-30"C(59-86*F)
2.Avoid freezing and excessive heat above 40°C(104°F)
Inactive Ingredients
Water (Aqua),Carbomer, Aminomethyl propanol Butylene glycol, Aloe barbadensis leaf extract
Package Label - Principal Display Panel
Undefined (Label)
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