Active Ingredient
Chloroxylenol 1.0% w/w
Afco 5508 Sanifect Foam-e Ii Liquid
FDA Label NDC 66949-141
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zep Inc. for the product Afco 5508 Sanifect Foam-e Ii (NDC 66949-141). 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, stop use and ask a doctor, 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
Antibacterial
Uses
- For handwashing to decrease bacteria on the skin.
- Recommended for repeated use.
Warnings
FOR EXTERNAL USE ONLY
When Using This Product
When using this product avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.
Stop Use And Ask A Doctor
Stop use and ask a doctor if if irritation or redness develops and persists.
Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact poison control center immediately.
Directions
- Wet hands with water, apply enough product to cover all hand surfaces, rub hands together for at least 30 seconds to work into lather.
- Rinse thoroughly and dry hands completely.
Other Information
For Food Processing, Food Service and Professional Use Only.
Inactive Ingredients
Water, Ammonium Lauryl Sulfate, Ethanol, Sodium Lauroyl Sarcosinate, Triethylene Glycol, Propylene Glycol, Glycerin, Disodium EDTA, Cocomidopropyl Hydroxysultaine, Citric Acid, Cocamide MIPA.
Questions Or Comments?
For product or technical information, contact ZEP, INC. Monday to Friday 8 AM to 4 PM EST at 1-877-428-9937 or visit our website at www.zep.com.
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