Active Ingredient
Ethyl Alcohol 75%(v/v)
Advanced Hand Sanitizer
FDA Label NDC 75151-001
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 Fuda Biotechnology Co., Ltd. for the product Advanced Hand Sanitizer (NDC 75151-001). 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, purpose, uses, warnings, when using this product, otc - stop use, 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
Antimicrobial
Uses
Hand sanitizer to help reduce bacteria on the skin.
Warnings
Flammable.Keep away from fire or flame.For external use only
When Using This Product
do not use in or near the eyes.In case of contact,rinse eyes thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if Irritation or rash appears and/or lasts
Keep Out Of Reach Of Children
If swallowed get medical help or contact a Poison Control Center right away
Directions
Put enough product in your palm to cover both hands and rub hands together briskly until dry.
Children under 6 years of age should be supervised when using this.
Other Information
Store below 110°F(43℃)
May discolor certain fabrics or surfaces
Inactive Ingredients
Purified water, Glycerin,Carbomer,Aminomethyl Propanol, Vitamin E
* Please review the disclaimer below.
