HAND SANITIZER- benzalkonium chloride liquid

Hand Sanitizer by

Drug Labeling and Warnings

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 skin
• recommended for repeated use

WARNINGS

Warnings

For external use only

WHEN USING

When using this product avoid contact with the 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 immediately.

DOSAGE & ADMINISTRATION

Directions

• apply liberally into palm of hand
• rub hands together until dry
• no need to rinse

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, FL 33133

www.tazzabrands.com

A Product of Terraboost® Made in USA [or Made in Taiwan] www.tazzabrands.com

PRINCIPAL DISPLAY PANEL

Tazza Instant Hand Sanitizer Foam

fragrance free

alcohol-free

Kills 99.99% of Germs

6000 PUMPS

81.15 Fl. OZ. (2,400mL)

INGREDIENTS AND APPEARANCE

HAND SANITIZER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76370-0002
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: 76370-0002-5	1000 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/27/2015
2	NDC: 76370-0002-6	2400 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/27/2015
3	NDC: 76370-0002-7	300 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/23/2020
4	NDC: 76370-0002-8	30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/23/2020
5	NDC: 76370-0002-9	500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/23/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	10/27/2015

Labeler - Terraboost Media LLC (831390047)