TAZZA-X HAND SANITIZING WIPES- ethanol cloth

Tazza-X Hand Sanitizing Wipes by

Drug Labeling and Warnings

Tazza-X Hand Sanitizing 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

Ethyl Alcohol 70%

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

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

STOP USE

Stop use and ask a doctor if irritation 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

• 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 ingredients Aloe Barbadensis Leaf Juice, Decyl Glucoside, Glycerin, Propylene Glycol, Purified Water

SPL UNCLASSIFIED SECTION

Made in China

Manufactured for Terraboost Media, LLC

3109 Grand Avenue #300

Miami, FL 33133

A product of Terraboost®

877-837-7210 www.tazzabrands.com

PRINCIPAL DISPLAY PANEL

tazza-X

HAND SANITIZING WIPES

70% alcohol formula

Kills Germs

180 Wet Wipes

5.11 in. x 7.08 in. (13cm x 18 cm)

INGREDIENTS AND APPEARANCE

TAZZA-X HAND SANITIZING WIPES 
ethanol cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76370-0008
Route of Administration	TOPICAL

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

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76370-0008-0	180 in 1 CANISTER	09/04/2020
1		1.3 mL in 1 APPLICATOR; Type 0: Not a Combination Product
2	NDC: 76370-0008-1	500 in 1 CANISTER	10/24/2020
2		1.3 mL in 1 APPLICATOR; Type 0: Not a Combination Product
3	NDC: 76370-0008-3	1200 in 1 CANISTER	10/24/2020
3		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)	09/04/2020

Labeler - Tazza Brands East Inc. (117842371)