Active Ingredient
Ethyl Alcohol 75%
Hand Sanitizer
FDA Label NDC 75749-017
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 Pretty Tourism Manufacture Co.,ltd. for the product Hand Sanitizer (NDC 75749-017). 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, 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 cause 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
Do not use on open skin wounds. in children less than 2 month of age.
When Using This Product
When using this product keep out of eyes, ears and mounth. In case of contact when eyes, rinse eyes thoroughly with water.
Stop Use
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 conatct a Posion 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.
Other Information
- Store between 15-30C (59-86F)
- Avoid freezing and excessive heat above 40C (104F).
Inactive Ingredients
Water(Aqua)
Triethanolamine,
Carbomer,
Glycerin,
Propylene glycol,
Aloe barbadensis extract,
Tocopheryl Acetate
Label
Label (Label)
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