Ozcare Antiseptic Hand Sanitizer
FDA Label NDC 75584-002

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Reed Holdings Australia, Pty. Ltd. for the product Ozcare Antiseptic Hand Sanitizer (NDC 75584-002). 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 active ingredient, purpose, use, warnings, do not use, 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

Use

  • for hand washing to decrease bacteria on the skin.

Warnings

For external use only
Flammable, keep away from fire or flame

Do Not Use

  • in the eyes

Stop Use And Ask A Doctor If

  • irritation and redness develop
  • if 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

Inactive Ingredients

Aloe Vera Extract, Disodium EDTA, Eucalyptus Oil, Glycerin, Lavender Oil, Tocopherol Acetate, Triethanolamine, Water

Questions Or Comments:

1-800-888-0776

Package Labeling:

Bottle (Bottle)

Bottle (Bottle)

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