Otc - Active Ingredient
Active ingredient
Ethanol 63% V/V
Tazza 63% Alcohol Foam Sanitizer Liquid
FDA Label NDC 76370-0042
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 63% Alcohol Foam Sanitizer (NDC 76370-0042). 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 - keep out of reach of children, otc - do not use, 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 Flammable: Keep away from flame or high heat.
For external use only
Otc - When Using
· When using this product keep out of eyes. Stop use and ask a doctor if redness or irritation 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.
Otc - Do Not Use
Do not use: on children under 2 years of age unless directed by a doctor.
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
Water, Cocamidopropylamine Oxide, Dimethicone, Propylene Glycol, Glycerine,Vitamin E
Package Label.Principal Display Panel
tazza 63% alcohol foam sanitizer 1L (33.8 FL OZ)
NDC: 76370-0042-0
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