TAZZA- benzalkonium chloride cloth

Tazza by

Drug Labeling and Warnings

Tazza by is a Otc medication manufactured, distributed, or labeled by Tazza Brands East Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

ACTIVE INGREDIENT

Active ingredient

Benzalkonium chloride 0.13%

PURPOSE

Purpose

Antiseptic

INDICATIONS & USAGE

Uses

• to decrease bacteria on the skin
• recommended for repeated use

WARNINGS

Warnings

For external use only

When using this product keep away from eyes. In case of eye contact, rinse eyes with water.

Stop use and ask a doctor if irritation or redness develop or last more than 72 hours.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions

• rub wipe thoroughly over all surfaces of both hands
• allow to dry without wiping
• supervise children under 6 years old
• not recommended for infants
• dispose of wipe in trash; do not fliush

INACTIVE INGREDIENT

Inactive ingredients Aloe Barbadensis Leaf Juice, Decyl Glucoside, Glycerin, Purified Water.

SPL UNCLASSIFIED SECTION

Made in China

Manufactured for Terraboost Media, LLC

3109 Grand Avenue #300

Miami, FL 33133

877-837-7210

A Product of Terraboost®

877-837-7210

www.tazzabrands.com

PRINCIPAL DISPLAY PANEL

tazza®

ANTISEPTIC HAND SANITIZING WIPES

Contains Benzalkonium Chloride

Alcohol-Free Formula

Kills germs.

1700 Wet Wipes

4.3 X 7.1" (11 cm X 18 cm)

INGREDIENTS AND APPEARANCE

TAZZA 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76370-0013
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76370-0013-0	1700 in 1 POUCH	06/09/2021
1		1.3 mL in 1 APPLICATOR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	06/09/2021

Labeler - Tazza Brands East Inc. (117842371)