Otc - Active Ingredient
Active Ingredient
Benzalkonium Chloride 0.13% w/v
Tazza Hand Sanitizer Liquid
FDA Label NDC 76370-0032
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 Hand Sanitizer (NDC 76370-0032). 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 For hand sanitizing to decrease bacteria on the skin.
Warnings
Warnings
· For external use only.
· When using this product avoid contact with eyes. In case of eye contact, flush eyes thoroughly with water.
· Stop use and ask a doctor if irritation or redness develops.
· Keep out of reach of children.
· If swallowed get medical help or contact Poison Control Center right away.
Otc - When Using
· When using this product avoid contact with eyes. In case of eye contact, flush eyes thoroughly with water.
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.
Dosage & Administration
Directions
· Apply and rub thoroughly over all surfaces of both hands.
· Allow to dry without wiping.
Inactive Ingredient
Inactive Ingredients
Purified Water, Glycerin, Aloe Barbadensis Leaf Juice, Decyl Glucoside.
Package Label.Principal Display Panel
1.0 Gallon
3.78 Liters
NDC: 76370-0032-0
* Please review the disclaimer below.
