Septihol Hand Sanitizer
Septihol Hand Sanitizer is an FDA drug label for the active ingredient ALCOHOL manufactured by STERIS Corporation administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20231206.
Generic: ALCOHOL
Manufacturer: STERIS Corporation
Product Type: HUMAN OTC DRUG
Route: TOPICAL
Dosage Form:
NDC: 0519-6257
Application: M003
Effective: 20231206
Active Ingredients: Active ingredient Ethyl Alcohol 62% v/v
Indications & Usage
Uses 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.
Dosage & Administration
Directions 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.
Contraindications
Not available.
Warnings
Warnings For external use only . Flammable, keep away from fire or flame. Do not puncture or incinerate. Do not store above 120ºF (49ºC). When using this product 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.
Adverse Reactions
Not available.
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