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Drug Facts
The following Structured Product Label (SPL) was submitted to the FDA by Steris Corporation for the product Septihol Hand Sanitizer (NDC 0519-6257). 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 other, active ingredient, purposes, uses, warnings, when using this product, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Drug Facts
Ethyl Alcohol 62% v/v
Antiseptic
To help decrease bacteria/germs on the skin that could cause disease. For use when soap and water are not available. Recommended for repeated use.
For external use only. Flammable, keep away from fire or flame. Do not puncture or incinerate. Do not store above 120°F (49°C).
Avoid contact with eyes. If splashed in eyes, rinse immediately and thoroughly with water. Do not use on open wounds, Discontinue use if irritation/redness occurs.
Stop use and ask a physician if irritation occurs for more than 3 days, contact a physician.
Keep out of reach of children. In case of ingestion, get medical help or contact a Poison Control Center immediately.
Spray product on hands, enough to cover all surfaces. Rub hands together until all surfaces are wet and fully covered. Continue rubbing until hands feel dry. Do not rinse or wipe off sanitizer.
For best foam density store and use at a temperature of 55 - 85˚F (13 - 29˚C)
Water, Hydrofluorocarbon 152a, Isobutane, Emulsifying Wax, Cetyl lactate, Steareth-2, Sodium Benzoate, Sodium Sesquicarbonate
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