Otc - Active Ingredient
Active ingredient
Alcohol 75% (w/w)
Ozlab Hand Sanitizer
FDA Label NDC 75531-004
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 75531-004). 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 - Purpose
Purpose - Antiseptic
Otc - Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Indications & Usage
For sanitizing and hand washing to decrease bacteria on skin
Warnings
For external use only: hands
Flammable. Keep away from heat, fire or spark, and electical.
Do not use near eyes. In case of contact, rinse eyes thoroughly with water Do not inhale or ingest.
Stop using and ask a doctor, if irritation or rash develops.
Dosage & Administration
Directions - Spray on palm generously (8-12 spprays), rub hands together and wet hands thoroughly with product. Allow at least 15 seconds for the product to kill germs.
Inactive Ingredient
Water (aqua), propylene glycol, Glycerin, Tocpheryl Acetate, fragrance (parfum)
* Please review the disclaimer below.
