Antibacterial Hand Sanitizer
FDA Label NDC 77879-002

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Bt Supplies West Inc for the product Antibacterial Hand Sanitizer (NDC 77879-002). 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.

Drug Facts

Active Ingredient

Ethyl Alcohol 73% v/v

Purpose

Antiseptic

Uses

  • For hand washing to help reduce bacteria that potentially can cause disease. Recommended for repeated use. For use  when soap and water are not available.

Warnings

For external use only.

Flammable. Keep away from fire 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 below 110°F (43°C).
  • May discolor ertain fabrics or surfaces.

Inactive Ingredients

Water, Glycerin, Squalane, Panthenol, Inulin, Sodium Hyaluronate, Fructose, Tocopheryl Acetate, Acrylates/C10-30Alkyl Acrylate Crosspolymer, Aminomethyl Propanol.

Package Labeling: 473Ml

Label1 (Label1)

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