Active Ingredient(S)
Ethyl Alcohol 60%
Alcohol Hand Sanitizer Liquid
FDA Label NDC 85279-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangdong Bangze Medicine Co., Ltd for the product Alcohol Hand Sanitizer (NDC 85279-001). 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
Antimicrobia
Use
Handsanitizer to help reduce bacteria on the skin.
Warnings
For external use only.
Do Not Use
Do not use near the eyesIn case of contact, rinse eyes thoroughly with water.
Otc - When Using
When using this product, do not use near the eyesln case of contact, rinse eyes thoroughly with water.
Otc - Stop Use
Stop useand askadoctorifir ritation or rash appears and lasts.
Otc - Keep Out Of Reach Of Children
Keepout of reach of children. If swallowed, get medical help orcontacta
Poison Control Center right away.
Directions
●Place enough product in your palm to thoroughly spread
onboth hands and rub into the skin until dry.
●Children under 6 years of age should be supervised when
using this porduct.
Other Information
●Store below 106'F (41°C)
●May discolor certain fabrics or surfaces
●Validity period after opening: 12 months
Inactive Ingredients
Water, Carbomer, Dandelion Extract, Winter FlowerExtract, Aminomethyl Propanol
Package Label - Principal Display Panel
Undefined (Label)
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