Otc - Active Ingredient
Active Ingredient
Ethyl Alcohol 72% v/v
Foaming Sanitizing Hand Soap
FDA Label NDC 50865-710
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Kutol Products Company for the product Foaming Sanitizing Hand (NDC 50865-710). 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, otc - purpose, otc - keep out of reach of children, indications & usage, dosage & administration, warnings, inactive ingredient, 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
Otc - Purpose
Purpose
Antibacterial
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, contact a physician or poison control center.
Indications & Usage
Uses Hand sanitizer to help reduce bacteria on the skin that could cause disease.
Dosage & Administration
Directions To decrease bacteria on skin, apply small amount to palm. Briskly rub, covering hands with product until dry.
Warnings
Warnings
For external use only.
FLAMMABLE. Keep away from heat or flames.
Avoid contact with eyes. If eye contact occurs, flush eyes with water.
Stop use if, in rare instances, redness or irritation develop. If condition persists for more than 72 hours, consult a physician.
Inactive Ingredient
Inactive Ingredients
water, cocamidopropyl PG-dimonium chloride phosphate,cocamidopropyl betaine, PEG-6 cocamide, laurtrimonium chloride, iodopropynyl butylcarbamate,methylisothiazolinone.
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