Hand Sanitizer Gel
FDA Label NDC 74177-021

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by K7 Design Group Inc. for the product Hand Sanitizer (NDC 74177-021). 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, use, 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

Alcohol 62%

Purpose

Antiseptic

Use

for hanw-ashing to decrease bacteria on the skin, only when water is not available

Warnings

For external use only
Flammable, keep away from fire and flames.

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 Contorl Center right away

Directions

  • Wet hands thoroughly with product and allow to dry without wiping

Inactive Ingredients

Water,Glycerin, Carbomer, Triethanolamine, Denatonium Benzoate.

Package Labeling:

Bottle (Bottle)

Bottle (Bottle)

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