Active Ingredient(S)
Ethyl Alcohol 70% v/v
The following Structured Product Label (SPL) was submitted to the FDA by Kova Laboratories, Inc. for the product Uhi Hand Sanitizer (NDC 79417-020). 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 active ingredient(s), purpose, use, warnings, do not use, otc - when using, 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.
Ethyl Alcohol 70% v/v
Antiseptic, Hand Sanitizer
For hand washing to decrease bacteria on the skin
For external use only. Flammable. Do not use near heat, flame or while smoking.
When using this product keep out of eyes. if product gets into eyes, rinse with water to remove. Avoid contact with broken skin. Do not inhale or ingest.
Stop use and ask a doctor if rash or irritation develops and lasts.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately
Do not store above 104F
May discolor some fabrics, wood finishes, and plastics
Water, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Propylene Glycol, Aloe Barbadensis Leaf Extract, PEG-8 Dimethicone, Triisopropanolamine, Linalool, FD&C Blue #1
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