Active Ingredients
80% Ethyl Alcohol
Hand Sanitizer
FDA Label NDC 75660-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Solvents And Petroleum Service, Inc. for the product Hand Sanitizer (NDC 75660-001). 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 ingredients, purpose, uses, warnings, otc - when using, otc - stop use, keep out of the reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Anticeptic
Uses
Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Warnings
For external use only - Hands. Flammable. Keep away from heat or flame
Otc - When Using
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep Out Of The Reach Of Children
Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Place enough product on hands to cover all surfaces. Rub hands together until dry.
Supervise children under 6 years of age when using this product to avoid swallowing.
Do not use on children less than 2 months of age. Do not use on open wounds.
Other Information
Store between 59-86F (15-30C)
Avoid freezing and excessive heat above 104F (40C)
Inactive Ingredients
glycerin, hydrogen peroxide, bittering agent, purified water USP
Package Label - Principal Display Panel
One Gallon NDC: 75660-001-01
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