Hand Sanitizer Gel
FDA Label NDC 79631-000

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Andaz Group Llc for the product Hand Sanitizer (NDC 79631-000). 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, 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 75%

Purpose

Antiseptic

Use

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

Warnings

For external use only.

Flammable, keep away from fire and flame.

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 Center right away.

Directions

wet hands thoroughly with product and allow to dry without wiping.

Other Information

  • Store below 105 °F
  • May discolor some fabrics.

Inactive Ingredients

Water, Carbomer, Aminomethyl Propanol.

Package Labeling:

Bottle (Bottle)

Bottle (Bottle)

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