Otc - Active Ingredient
Ethyl Alcohol - 76%
Zylast Antiseptic Gel
FDA Label NDC 57362-465
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Innovative Biodefense for the product Zylast Antiseptic (NDC 57362-465). 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 - ask doctor, otc - keep out of reach of children, dosage & administration, warnings, inactive ingredient, indications & usage, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Antiseptic
Otc - Ask Doctor
Discontinue use if irritation and redness develops. Consult a doctor if condition persists for more than 72 hours.
Otc - Keep Out Of Reach Of Children
If swallowed, immediately call Poison Control Center or doctor.
Dosage & Administration
We hands thoroughly with product and allow to dry without wiping.
Warnings
For external use only. Flammable, keep away from flame. Avoid contact with eyes. In case of eye contact, rinse eyes thoroughly with water.Consult a doctor if condition persists for more than 72 hours.
Inactive Ingredient
Water, Polyaminopropyl Biguanide, Panthenol, Hydroxyethyl Ethylcellulose, Farnesol, PEG-12, Dimethicone, Benzethonium Chloride.
Indications & Usage
Handwash to decrease bacteria on the skin that potentially can cause disease. Recommended for repeated use.
* Please review the disclaimer below.
