Hand Sanitizer
FDA Label NDC 76924-000

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by General Organics Inc. for the product Hand Sanitizer (NDC 76924-000). 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 a 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

Active Ingredient

Ethyl Alcohol 70%

Purpose

Antiseptic

Uses

for hand-washing to decrease bacteria on the skin, only when water is not available

Warnings

  • Flammable, keep away from fire and flames
  • For external use ony

When Using This Product

  • do not get into eyes
  • if contact occurs, rinse eyes thoroughly with water

Stop Use And Ask A Doctor If

  • irritation and redness develop

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Cente right away.

Directions

  • wet hand thoroughly with product and allow to dry without wiping.

Inactive Ingredients

water, triethanolamine, carbopol, tween 20, glycerin, aloe

Package Labeling:

Label (Label)

Label (Label)

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