Active Ingredient
Ethyl Alcohol 62% v/v
Amcon Labs Hand Sanitizer Instant Foam Sanitizer With Alcohol Solution
FDA Label NDC 51801-366
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Nomax, Inc. for the product Amcon Labs Hand Sanitizer Instant Foam Sanitizer With Alcohol (NDC 51801-366). 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, use, warnings, otc - keep out of reach of children, directions, inactive ingredients, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Skin Sanitizer
Use
To help reduce the amount of bacteria on skin
Warnings
Flammable. Keep away from fire or flame.
For external use only. If swallowed, seek medical attention.
When using this product do not use around or near the eyes. If contact occurs, flush eyes with water and contact a doctor immediately.
Stop use and consult a doctor when skin irritation appears and lasts.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Directions
- Pump a small amount of foam into palm of hand.
- Spread on hands and rub into skin until dry.
- Pump a smaller amount into one hand and spread over both hands and wrists.
- Rub into skin until dry.
- Children should be supervised while using this product.
Inactive Ingredients
Water, Acrylates/Perfluorohexylethyl Methacrylate Copolymer, Perfluorohexylethyl Alcohol, Glycerin, Aloe Barbadensis Leaf Juice
Package Label.Principal Display Panel
Product Label (550 mL)
* Please review the disclaimer below.
