Active Ingredients:
Ethyl Alcohol 80%
Azx Wellness Hand Sanitizer Gel
FDA Label NDC 73145-007
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Asc Marketing Ltd for the product Azx Wellness Hand Sanitizer (NDC 73145-007). 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 ingredients:, purpose:, uses, warnings, do not use, stop use and ask a doctor, 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
Purpose:
Antiseptic
Uses
For hand washing to decrease bacteria on the skin.
Warnings
For external use only. Flammable. Keep away from fire or flames.
Do Not Use
in the eyes. In case of contact, rinse eyes thoroughly with water.
Stop Use And Ask A Doctor
if irritation or redness develop and persist for more than 72 hours.
Keep Out Of Reach Of Children.
If swallowed get medical help or contact Poison Control Center right away. Store between 59-86°F (15-30°C). Avoid freezing and excessive heat above 104°F (40°C).
Directions
Wet hands thoroughly for at least 20 seconds with product and allow to dry without wiping. Supervise children in the use of this product.
Inactive Ingredients
GLYCERIN, HYDROGEN PEROXIDE, METHYLCELLULOSE, STERILE WATER.
* Please review the disclaimer below.
