AFCO 5508 Sanifect Foam-E II
Chloroxylenol · Liquid · Topical
Active ingredient
Active ingredient Chloroxylenol 1.0% w/w
Purpose
Purpose Antiseptic
Uses
Uses Hand wash to help reduce bacteria on skin that potentially can cause diseases. Helps prevent cross contamination by hand contact. Recommended for repeat use.
Warnings
Warnings For external use only – Harmful if swallowed.
When using this product
When using this product When using this product do not use in or near eyes. If eye contact occurs, rinse eyes thoroughly with water. Discontinue use if irritation or redness develops.
Stop use and ask a doctor
Stop use and ask a doctor Stop use and ask a doctor if skin irritation or redness persists for more than 72 hours.
Keep out of reach of children
Keep out of reach of children Keep out of reach of children. In case of accidental ingestion, seek medical attention or contact poison control center immediately.
Directions
Directions For one step hand washing and sanitizing, wet hands with water. Apply a generous amount of product in palm of hand and work into later. Rinse thoroughly with potable water. Dry hands completely.
Inactive ingredients
Inactive ingredients Water, Ammonium Lauryl Sulfate, Ammonium Laureth Sulfate, Ethyl Alcohol, Propylene Glycol, Cocamide MEA, Glycerin, Disodium EDTA.
Questions?
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.
Label text from the FDA structured product label by Zep Inc. (revised Dec 26, 2025). Long sections are shortened; the complete label is on DailyMed.
Active ingredients
- Chloroxylenol in 2 products
AFCO 5508 Sanifect Foam-E II NDC products (2)
Frequently asked questions
What is AFCO 5508 Sanifect Foam-E II used for?
Uses Hand wash to help reduce bacteria on skin that potentially can cause diseases. Helps prevent cross contamination by hand contact. Recommended for repeat use.
Who makes AFCO 5508 Sanifect Foam-E II?
AFCO 5508 Sanifect Foam-E II is listed by 1 labeler in the FDA NDC directory, including Zep Inc..