Active Ingredient(S)
Alcohol 67.0%
Instant Hand Sanitizer
FDA Label NDC 79744-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Hangzhou Keon Biotech Co., Ltd. for the product Instant Hand Sanitizer (NDC 79744-001). 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, do not use, otc - when using, otc - stop use, 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
Antimicrobial
Use
Use for hand-washing to decrease bacteria on the skin, only when wafer is not available.
Warnings
Warnings Flammable, keep away from fire and flame. For external use only.
Do Not Use
/
Otc - When Using
When using this product Do not get into eyes.
If contact occurs, rinse eyes thoroughly witti water. May discolor some fabrics.
Otc - Stop Use
Stop use and ask a doctor if Irritation and redness develop.
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
Directions wet hands thoroughly with product and allow to dry without wiping
Other Information
Other information store below 1os °F
Inactive Ingredients
AQUA, GLYCERIN, CARBOMER, TRIETHANOLAMINE
* Please review the disclaimer below.
