TAZZA HAND SANITIZER GYM WIPES- benzalkonium chloride cloth

Tazza Hand Sanitizer by

Drug Labeling and Warnings

Tazza Hand Sanitizer 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 productavoid contact with eyes. In case of contact, flush eyes thoroughly with water.

STOP USE

Stop use and ask a doctor ifirritation or redness develop or last more than 72 hours

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 in trash; do not flush

INACTIVE INGREDIENT

Inactive ingredientsWater, Ethyl Alcohol, Acetic Acid (Vinegar), Cocamidopropyl Betaine, Decyl Glucoside, Phenoxyethanol, Acrylates Copolymer, Aloe Barbadensis Leaf Extract,

SPL UNCLASSIFIED SECTION

Made in China

Manufactured for

Tazza Brands East

4140 Mound Road

Joliet, IL 60436

PRINCIPAL DISPLAY PANEL

1500 Wet Wipes / XL SIZE

7in x 5in (17.7cm x 12.7cm)
NDC: 76370-0017-0

INGREDIENTS AND APPEARANCE

TAZZA HAND SANITIZER  GYM WIPES
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76370-0017
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
ACETIC ACID (UNII: Q40Q9N063P)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76370-0017-0	1500 in 1 BAG	06/10/2022
1		1.1 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)	06/10/2022

Labeler - Tazza Brands East Inc (117842371)

Registrant - Tazza Brands East Inc (117842371)