Active Ingredient(S)
Alcohol 62%
Hand Sanitizer
FDA Label NDC 79867-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangzhou Meizi Biotechnology Co. Ltd for the product Hand Sanitizer (NDC 79867-001). 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
Antiseptic
Use
For handwashing to decrease bacteria on the skin
Warnings
For external use only.
Flammable keep away from fre or flame.
Do Not Use
Do not use near eyes,in case of contact flush eyes with water
Otc - When Using
Do not use near eyes,in case of contact flush eyes with water
Otc - Stop Use
Redness or irritationdevelops
Persists for morehan 72 hours
Otc - Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away
Directions
Place a palmful (5 grams)of product in one hand. spread on both hands and rub into skin until dry (1-2 min）
Children must be supervised in the use of this products.
Other Information
Store below105F°
May discolor fabrics
Inactive Ingredients
Water, Glycerin, Propylene Glycol, carbomer, Triethanolamine
Package Label - Principal Display Panel
29 (29)
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