Active Ingredient(S)
Ethyl Alcohol 75% v/v
Hand Sanitizer Wipes
FDA Label NDC 42129-015
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Fustin(xiamen) Commodity Co., Ltd for the product Hand Sanitizer Wipes (NDC 42129-015). 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, otc - keep out of reach of children, otc - when using, do not use, otc - stop use, 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 wipes help reduce bacteria that potentially can cause disease. For use when soap and water are not available
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
Otc - When Using
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Do Not Use
In children less than 2 months of age On open skin wounds
Otc - Stop Use
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition
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
Inactive Ingredients
Water, Aloe Vera Extract, Honeysuckle Extract
Storage And Handling
Store between 15-30°C(59-86°F)
Avoid freezing and excessive heat above 40°C(104°F)
Package Label - Principal Display Panel
1 (Cshandwipe50)
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