Other
NA
Maximum Hand Sanitizer
FDA Label NDC 76114-003
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 Aidi Cosmetics Co., Ltd for the product Maximum Hand Sanitizer (NDC 76114-003). 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 other, active ingredient(s), purpose, use, warnings, 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
Active Ingredient(S)
Ethyl Alcohol 70% v/v
Purpose
Antiseptic
Use
Hand sanitizer to help reduce bacteria on the skin
Warnings
Flammable. Keep away from fire or flame
For external use only.
Otc - When Using
When using this product do not use in or near the eyes. In case of contact with eyes, rinse eyes thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if irritation or redness develops
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
Appply to palm of hands. Rub hands together vigorously untill dry.
Supervise chirldren in the use of this product.
Other Information
Do not store above 110F (43C)
May discolor certain fabrics or surfaces
Inactive Ingredients
Water, triethanolamine, carbomer, aloe barbadensis (Aloe vera) gel, fragrance, propylene glycol, glycerin, tocopheryl acetate (Vitamin E)
Package Label.Principal Display Panel
Image Description (Electronic)
* Please review the disclaimer below.
