Urigel Neutro Antiseptic Hand Sanitize 75%r 75%
FDA Label NDC 80924-003

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Urigel Inc. for the product Urigel Neutro Antiseptic Hand Sanitize 75%r 75% (NDC 80924-003). 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, use, warnings, do not use, stop use and ask a doctor if:, 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 80%

Purpose

Antiseptic

Use

For hand washing to decrease bacteria on the skin

Warnings

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

Do Not Use

in the eyes.

Stop Use And Ask A Doctor If:

  • irritation and redness develop.
  • condition persists for more than 72 hours.

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 between 59-86°F (15-30°C) 
  • Avoid freezing and excessive heat above 104°F (40°C)

Inactive Ingredients

Glycerin, hydrogen peroxide, water.

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