AFCO 5508 Sanifect Foam-E II 2081980 mg/208198mL
Chloroxylenol · LIQUID · Zep Inc.
AFCO 5508 Sanifect Foam-E II is a liquid containing chloroxylenol at 2081980 mg/208198mL, taken topical. Manufactured by Zep Inc..
Key Facts
- Brand Name
- AFCO 5508 Sanifect Foam-E II
- Generic Name
- Chloroxylenol
- NDC Code (Product)
66949-141- Manufacturer
- Zep Inc.
- Strength
- 2081980 mg/208198mL
- Dosage Form
- LIQUID
- Route
- TOPICAL
- Marketing Status
- Application #
- 505G(a)(3)
- Marketing Start
- 10/23/2025
Recall History
No Recall HistorySide Effects Reported to FDA
FDA FAERS database · These are reported events, not confirmed side effects
Full Prescribing Information
Indications & Usage
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.
Dosage & Administration
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.
Warnings
Warnings For external use only – Harmful if swallowed.
Frequently Asked Questions
What is AFCO 5508 Sanifect Foam-E II used for?
AFCO 5508 Sanifect Foam-E II contains Chloroxylenol. It is a liquid taken topical. Consult your doctor for specific uses.
Is AFCO 5508 Sanifect Foam-E II a controlled substance?
AFCO 5508 Sanifect Foam-E II is not classified as a controlled substance by the DEA.
What is the generic name for AFCO 5508 Sanifect Foam-E II?
The generic name for AFCO 5508 Sanifect Foam-E II is Chloroxylenol. There are 12 other brand versions of Chloroxylenol.
What is the NDC code for AFCO 5508 Sanifect Foam-E II 2081980 mg/208198mL?
The NDC (National Drug Code) for AFCO 5508 Sanifect Foam-E II 2081980 mg/208198mL is 66949-141, listed by Zep Inc..
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Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)