Active Ingredient
Alcohol 58%
Upw Hand Sanitizer
FDA Label NDC 80138-203
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Kumsung Enc Co., Ltd for the product Upw Hand Sanitizer (NDC 80138-203). 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, when using this product, stop use and ask a doctor, keep out of reach of children., 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 to help reduce bacteria on the skin. For use when soap and water are not available.
Warnings
For external use only. Flammable. Keep away form heat or flame
Do not use
- on infants less 2months of age
- on open skin wounds
When Using This Product
keep away from eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
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 contact a Poison 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 1~30℃(33.8~86℉)
- Avoid freezing and excessive heat above 40℃(104℉)
Inactive Ingredients
glycerin, 1,3-butylene glycol, carbomer940, triethanol amine, purified water USP
Package Label
* Please review the disclaimer below.
