Active Ingredient
Ethyl Alcohol 75%
Alcohol Wipes
FDA Label NDC 75749-051
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 Alcohol Wipes (NDC 75749-051). 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 and ask a doctor, 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
Anitbacterial
Use
decrease bacteria on skin
Warnings
For external use only.
Do Not Use
If you are allergic to any of the ingredients
When Using This Product
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop Use And Ask A Doctor
Stop use and ask a doctor if irritation or rash occurs develops and continues for more than 72 hours
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
adult and children 2years and over
- apply to hands
- allow to dry without wiping
- ask a doctor before use
children under 2 years
Inactive Ingredients
Water
Glycerin
Aloe barbadensis extract
* Please review the disclaimer below.
