Beis Advanced Hand Sanitizer (promotional)
FDA Label NDC 81263-004
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Beis Llc for the product Beis Advanced Hand Sanitizer (promotional) (NDC 81263-004). 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 drug facts, active ingredient, purpose, uses, warnings, when using this product, stop use and ask a doctor, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Ethyl Alcohol 75% v/v
Purpose
Antiseptic
Uses
- For hand washing to help reduce bacteria that potentially can cuase disease. Recommended for repeated use. For use when soap and water are not available.
Warnings
For external use only
Flammable. Keep away from heat or flame
When Using This Product
do not use in or near 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 appears on the skin.
Keep Out Of 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.
- Children under 6 years of age should be supervised by adult when applying this product.
- Do not use on children less than 2 months of age or on open skin wounds.
Other Information
- Store between 15-30°C (59-86°F)
- Avoid freezing and excessive heat above 40°C (104°F)
- May discolor some fabrics or surfaces
Inactive Ingredients
Water, Glycerin, Squalane, Panthenol, Inulin, Sodium Hyaluronate, Fructose, Tocopheryl Acetate, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol.
Package Labeling:
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