TAZZA ANTISEPTIC HAND WIPES- isopropyl alcohol cloth

Tazza Antiseptic Hand Wipes by

Drug Labeling and Warnings

Tazza Antiseptic Hand Wipes 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

Isopropyl Alcohol 75%

PURPOSE

Purpose

Antiseptic

INDICATIONS & USAGE

Uses

• 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 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 immediately.

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 flush

STORAGE AND HANDLING

Other information

• store below 100°F (38°C)
• non-staining; may discolor some fabrics

INACTIVE INGREDIENT

Inactive ingredient

Water

SPL UNCLASSIFIED SECTION

Made in China

Manufactured for:
Tazza Brands East, Inc.
2232 Dell Range Blvd
Suite 202
Cheyenne, WY 82009
A Product of Terraboost®
877-837-7210
www.tazzabrands.com

PRINCIPAL DISPLAY PANEL

tazza®

75% ISOPROPYL ALCOHOL

ANTISEPTIC HAND SANITIZING WIPES

Kills germs

1000 Heavy Duty Presaturated Disposable Wipes

6 in x 8 in (15.24cm x 20.32cm)

NDC: 76370-0012-0

INGREDIENTS AND APPEARANCE

TAZZA ANTISEPTIC HAND WIPES 
isopropyl alcohol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76370-0012
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302)	ISOPROPYL ALCOHOL	75 mL  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76370-0012-0	1000 in 1 POUCH	05/29/2021
1		3.7 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)	05/29/2021

Labeler - Tazza Brands East Inc. (117842371)