Otc - Active Ingredient
Active Ingredient
Ethanol 70%V/V
Tazza 70% Alcohol-based Hand Sanitizing Foam Liquid
FDA Label NDC 76370-0033
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 70% Alcohol-based Hand Sanitizing Foam (NDC 76370-0033). 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
Antiseptic
Indications & Usage
Uses ·for hand sanitizing to decrease bacteria on the skin
·recommended for repeated use
Warnings
Warnings
For external use only
Flammable.Keep away from fire or flame.
Otc - When Using
When using this product avoid contact with the eyes.In case of contact,
flush eyes thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if irritation or redness develop
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 ·apply liberally into palm of hand
·rub hands together until dry ·no need to rinse
Storage And Handling
Other information ·do not store above 100°F(38℃)
·non-staining ·may discolor some fabrics
Inactive Ingredient
Inactive ingredients Water, Cocamidopropylamine Oxide, Dimethicone,
Propylene Glycol, Glycerine, Vitamin E
Package Label.Principal Display Panel
Tazza
70% Alcohol-Based Hand Sanitizing Foam
1 Gallon bottle
NDC: 76370-0033-0
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