Active Ingredient(S)
Ethyl Alcohol .......... 75% v/v.
Hand Sanitizing
FDA Label NDC 75329-1001
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 Lizi Commodity Co., Ltd. for the product Hand Sanitizing (NDC 75329-1001). 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
Premiun sanitizer to reduce 99.9% of most illness-causing germs and bacteria. Antiseptic for hands and skin. Sanitize and disinfect hands and skin 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 or puncture-type wounds.
Otc - When Using
Otc - Stop Use
Stop use and ask a doctor if irritation appears.
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.
Direction
Clean hands annd skin with by spraying on hands and skin and gently rubbing No need to rinse, let hands or skin dry
Other Information
read all directions and warnings before using
Store at room temperature 15℃ to 34℃ （59 ℉ to 86℉）with package closed.
Avoid excessive heat above 40℃ (114℉）
Inactive Ingredients
Aqua (Purified Water), Glycerinum
* Please review the disclaimer below.
