Active Ingredient(S)
Ethyl Alcohol 62% v/v
Antibacterial Hand Sanitizer
FDA Label NDC 76114-011
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 Antibacterial Hand Sanitizer (NDC 76114-011). 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
Antiseptic
Use
Hand sanitizer to help decrease bacteria on the skin
When water, soap, and towel are not available
Recommended for repeaded use
Warnings
For external use only.
Flammable. Keep away from fire or flame
Do not apply around eyes. Do not use in ears and mouth
Otc - When Using
When using this product avoid contact with eyes. In case of contact, flush eyes with water.
Otc - Stop Use
Stop use and ask a doctor if redness or irritation develops and persists for more than 72 hours
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. Children must be supervised in use of this product.
Directions
Squirt as needed into your palms and thoroughly spread on both hands, rub into skin until dry
Other Information
Store at 20C (68-77F)
May discolor fabrics
Inactive Ingredients
Water, triethanolamine, carbomer, fragrance, glycerin, tocopheryl acetate (Vitamin E), Aloe barbadensis leaf extract
* Please review the disclaimer below.
