Ozlab Hand Sanitizer
FDA Label NDC 75531-006

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Zhejiang Ounuo Cosmetics Co., Ltd. for the product Ozlab Hand Sanitizer (NDC 75531-006). 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 otc - active ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Otc - Active Ingredient

Active ingredient                                  Purpose

Alcohol                75% (w/w)      ...        Antiseptic

Otc - Purpose

  • to kill germs and bacteria.
  • recommended for repeated use.

Otc - Keep Out Of Reach Of Children

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

Indications & Usage

keep out of eyes

Warnings

For external use only: hands
Flammable. Keep away from fire or flame.

When using this products, keep out of eyes.

Stop using and ask a doctor, if irritation or redness develops.

Dosage & Administration

  • Wet hands thoroughly with product andd rub until dry.

Inactive Ingredient

Water (aqua), propylene glycol, Glycerin, acrylates/c10-30 alkyl acrylate crosspolymer, aminomethyl Propanol, aloe barbadensis leaf extract, fragrance (parfum)

* Please review the disclaimer below.