Otc - Active Ingredient
Active ingredient
Benzalkonium Chloride 0.13% w/v
Tazza Alcohol-free Sanitizer Liquid
FDA Label NDC 76370-0041
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Tazza Brands East Inc. for the product Tazza Alcohol-free Sanitizer (NDC 76370-0041). 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, indications & usage, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Purpose
Antimicrobial
Indications & Usage
Uses · Decreases bacteria on hands
Warnings
Warnings
For external use only.
Otc - When Using
· When using this product keep out of eyes.
Otc - Stop Use
Stop use and ask a doctor if irritation or redness develops.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center Immediately.
Dosage & Administration
Directions
· Dispense an adequate amount in your palm to cover all surfaces of both hands completely · Rub hands together until dry.
Storage And Handling
Other information · Store at room temperature.
· Avoid excessive heat.
Inactive Ingredient
Inactive Ingredients
Purified water, Glycerin, Aloe Barbadensis Leaf Juice, Decyl Glucoside.
Package Label.Principal Display Panel
tazza Alcohol-Free sanitizer 1L (33.8 FL OZ)
NDC: 76370-0041-0
* Please review the disclaimer below.
