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Drug Facts
Distributed by Spectrum
Division of United Industries Corporation
PO Box 142642, St. Louis, MO 63114-0642
The following Structured Product Label (SPL) was submitted to the FDA by United Industries Corporation for the product Cutter Brand Hand Sanitizer (NDC 79364-1682). 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, purpose, use, warnings, do not use, otc - when using, otc - stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Drug Facts
Distributed by Spectrum
Division of United Industries Corporation
PO Box 142642, St. Louis, MO 63114-0642
Ethyl Alcohol 77% (v/v)
Antiseptic
Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
For external use only.
When using this product keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Aloe Barbadensis Leaf Juice, Ammonium Acryloyldimethyltaurate/VP Copolymer, Caprylic/Capric Triglyceride, Hydroxyethyl Urea, Tocopheryl Acetate, Water.
Call 1-888-837-6688 or visit our website at www.cutterprotects.com
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