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Antibacterial Hand Sanitizer
FDA Label NDC 81131-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Hubei Flex Daily Chemicals Co., Ltd for the product Antibacterial Hand Sanitizer (NDC 81131-001). 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 other, active ingredient(s), purpose, use, warnings, otc - when using, 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
Active Ingredient(S)
Ethyl Alcohol 62%.
Purpose
Antiseptic
Use
Hand sanitizer to help decrease bacterial on the skkin when water, soap and towel are not available
Recommended for repeated 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
Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. Children must be spervised when use this product.
Directions
Squirt as needed into your palms and thoroughly spread on both hands, rub into skin until dry.
Other Information
Store st 20C (68-77F)
May discolor some fabrics
Inactive Ingredients
Water, glycerin, triethanolamine, carbomer, Vitamin E, aloe barbadensis leaf extract
Package Label.Principal Display Panel
Image Description (60ml)
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