TAZZA 70% ALCOHOL-BASED HAND SANITIZING FOAM- alcohol liquid

Tazza 70% Alcohol-Based Hand Sanitizing Foam by

Drug Labeling and Warnings

Tazza 70% Alcohol-Based Hand Sanitizing Foam by is a Otc medication manufactured, distributed, or labeled by Tazza Brands East, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredient

Ethanol 70%V/V

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.

WHEN USING

When using this product avoid contact with the eyes.In case of contact,

flush eyes thoroughly with water.

STOP USE

Stop use and ask a doctor if irritation or redness develop

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

PRINCIPAL DISPLAY PANEL

Tazza
70% Alcohol-Based Hand Sanitizing Foam
1 Gallon bottle
NDC: 76370-0033-0

INGREDIENTS AND APPEARANCE

TAZZA 70% ALCOHOL-BASED HAND SANITIZING FOAM 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76370-0033
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	70 L  in 100 L

Inactive Ingredients
Ingredient Name	Strength
COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)
WATER (UNII: 059QF0KO0R)
DIMETHICONE (UNII: 92RU3N3Y1O)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
.ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76370-0033-0	3.785 L in 1 BOTTLE; Type 0: Not a Combination Product	04/18/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	04/18/2025

Labeler - Tazza Brands East, Inc. (117842371)