Otc - Active Ingredient
Ethjyl Alcohol
Advanced Alcohol Foaming Hand Sanitizer Liquid
FDA Label NDC 65601-802
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Betco Corporation Llc for the product Advanced Alcohol Foaming Hand Sanitizer (NDC 65601-802). 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 otc - active ingredient, inactives, dosage, usage, purpose, keep out of reach, warnings, package label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactives
Aloe Barbadensis Leaf Juice, D&C Green #5, PEG 10 Perfluorohexylethyl acrylate copolymer, Perluorohexylethyl alcohol, propylene glycol, water
Dosage
Please read entire label before using thsi product. Place enough product on your palm to tnoroughly cover your hands, Rub hands together briskyl until dry.
Usage
Hand sanitizer to reduce mocroorganisms on the skin.. Use this product when soap and water are not available.
Purpose
Antiseptic
Keep Out Of Reach
Keep out of reach of children. If swallowed get medical help or contact a Poison Control center right away.
Warnings
For external use only. FLAMMABLE. This product contains ethyl alcohol. Keep away from heat or flame.
When using this product avoid contact with eyes. If contact occurs rinse thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs.
Package Label
Product Label (79529 00 Advance Alcohol Foaming Sanitizer)
* Please review the disclaimer below.
