Active Ingredient(S)
Ethyl Alcohol 70%
U Instant Hand Sanitizer Classic
FDA Label NDC 75112-006
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zhejiang Shenying Technology Co., Ltd. Jiaojiang Branch for the product U Instant Hand Sanitizer Classic (NDC 75112-006). 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, otc - when using, otc - stop use, otc - 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
Antimicrobial
Use
Hand sanitizer to help reduce bacteria on the skin
Warnings
For external use only
Flammable. Keep away from fire or flame
Otc - When Using
When using this product do not use in or near eyes. In case of eye contact, rinse eyes thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if irritation or rash appears and lasts
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.
Directions
Place enough product in your palm to thoroughly spread on both hands and rub into skin untill dry
Children under six years of age should be supervised when using this product
Other Information
Store below 106F (41C)
May discolor certain fabrics or surfaces
Inactive Ingredients
Water, aloe barbadensis leaf jiuce, carbomer, fragrance, glycerin, propylene glycol, triethanolamine, tocopheryl acetate, 2-(dimethylamino) ethanol
Package Label.Principal Display Panel
Image Description (Img 5535)
* Please review the disclaimer below.
