Active Ingredient
Ethyl Alcohol 75%V/V
Hand Sanitizer
FDA Label NDC 52807-022
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangdong Longtai Industry Co.,ltd for the product Hand Sanitizer (NDC 52807-022). 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, warnings, do not use, otc - when using, other information, indications & usage, 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
Purpose: Antimicrobial
Warnings
For external use only.
flammable, keep away from fire or fame
Do Not Use
in children less than 2 months of age
open skin wounds
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.
Other Information
Store between 20°C to 25°C (68°F to 77°F)
Indications & Usage
Hand santizer to 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
Inactive Ingredient
Aloe Barbadensis Leaf Extract, Aminomethyl Popanol, Carbomer, Glycerin, Tocopheryl Acetate, Water
Dosage & Administration
Place enough product on hands to cover all surfaces
Rub hands together until dry
Supervise children under B years of age when using this product to avoid swallowing
Otc - Stop Use
Stop use and aska doctor if irritation or rash occurs. These may be signs of a serious condition
* Please review the disclaimer below.
