Active Ingredient
Ethyl alcohol 80% v/v
Premier Pure Protection
FDA Label NDC 73945-007
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Rpp Products, Inc. for the product Premier Pure Protection (NDC 73945-007). 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, purpose, uses, warnings, when using this product, stop use and ask doctor if, keep out of 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
Antimicrobial
Uses
Sanitizer to help reduce bacteria and germs on hands.
For use when soap and water are not available.
Warnings
Flammable, keep away from fire or flame
For external use only
When Using This Product
do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water
Stop Use And Ask Doctor If
irritation or rash appears and lasts
Keep Out Of Reach Of Children.
If swallowed, get medical help right away or contact a Poison Control Center immediately.
Directions
- Spray enough product to completly moisten and wipe clean until dry.
- children under 12 years of age should be supervised when using this PREMIER PURE
Other Information
- Store below 1100 F (430C)
- May discolor certain fabrics or surfaces
- This product does not contain any chemicals known to the State of California to cause cancer, birth defects, or any other reproductive harm
Inactive Ingredients
Water, Isopropyl Alcohol, Glycerin, Tert-butyl Alcohol, Denatonium Benzoate
Product Label
Image Description (Front)
Image Description (Back)
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