Otc - Active Ingredient
Ethyl Alcohol - 76%
Zylast Antiseptic S Liquid
FDA Label NDC 57362-466
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 S (NDC 57362-466). 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, directions, warning section, inactive ingredient, uses, 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.
Directions
Place enough product on hands to completely spread over both hands and wrists, paying attention to nails, cuticles and inderdigital spaces. Rub into skin until dry.
Warning Section
For external use only. Flammable, keep away from flame. Avoid contact with eyes. In case of eye contact, rinse eyes thoroughly with water. Discontinue use if irritation and redness develops.
Inactive Ingredient
Water, Polyaminopropyl Biguanide, Panthenol, Hydroxyethyl Ethylcellulose, Farnesol, PEG-12, Dimethicone, Benzethonium Chloride
Uses
Significantly reduces the number of micro-organisms on the hands and forearms. Decreaes bacteria on the skin that can potentially cause disease. Recommended for repeated use.
Package Label.Principal Display Panel
NDC 57702-466-16
Zylast Antiseptic S
1000mL
Broad Spectrum
Antimicrobial
* Please review the disclaimer below.
