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

Antimicrobial

INDICATIONS & USAGE

Uses

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

WARNINGS

Warnings

For external use only

WHEN USING

When using this product avoid contact with eyes. In case of eye contact, flush eyes 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 right away.

DOSAGE & ADMINISTRATION

Directions

• take wipe and rub thoroughly over all surfaces of both hands
• rub hands together briskly to dry
• dispose of wipe

INACTIVE INGREDIENT

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

SPL UNCLASSIFIED SECTION

Manufactured for Terraboost Media, LLC
3109 Grand Avenue #300, Miami, DL 33133

Questions? Tazza Brands:

877-837-7210

www.tazzabrands.com

MADE IN USA

PRINCIPAL DISPLAY PANEL

tazza®

ANTISEPTIC

HAND SANITIZING WIPES

Contains Benzalkonium Chloride

Alcohol-Free Formula

Kills 99.99% of most common germs

1200 Wet Wipes

4.25" x 6.75" (10.8 cm x 17.2 cm)

INGREDIENTS AND APPEARANCE

TAZZA 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76370-0009
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: 76370-0009-0	500 in 1 CANISTER	10/24/2020
1		1.3 mL in 1 APPLICATOR; Type 0: Not a Combination Product
2	NDC: 76370-0009-1	1200 in 1 CANISTER	10/24/2020
2		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)	10/24/2020

Labeler - Tazza Brands East Inc. (117842371)