Q SHIELD- benzalkonium chloride liquid

Q Shield by

Drug Labeling and Warnings

Q Shield by is a Otc medication manufactured, distributed, or labeled by Pierce Innovations, LLC, Fill Tech USA, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.13%

Purpose

Hand & Skin Antiseptic

Uses

Hand & Skin Antiseptic to help decrease pathogens (germs) on the skin.

Warnings

For external use only.

Do not use

• if you are allergic to any of our ingredients
• in your ears, mouth, or eyes.
• If eye contact occurs, rinse thoroughly with water.

Ask a doctor before use if you have

• open wounds.
• serious burns.

Stop use and ask doctor if

• redness or skin irritation develop after use, and persists for more than 72 hours.

Keep out of reach of children

• Children should be supervised when using this product.

Directions

Apply (3) (1) pump(s) onto clean, dry hands. Ensure coverage on skin and under fingernails.

Inactive ingredients

1-Octadecyldimethyl (3-Trimethoxysilylpropyl) ammonium chloride, deionized water, and ethanol

Questions?

Call 1-833-700-0111

Principal Display Panel

Axenic Hand(tm)

Q Shield(tm)

Patented, Non-Toxic, Medical-grade Formula

Persistent Hand Disinfectant

Gentle on Hands

Extended Protection

Full Spectrum

40 Days of Full Coverage Per Bottle

Made in USA

(Distributed by:) (Manufactured for:)

Pierce Innovations, LLC

4578 Jonathan Creek Road

Waynesville, NC 28785

Manufactured in the USA at FDA-GMP Facilities

For additional product details, please call 1-833-747-8283 or visit our site online at www.axenichealthsolutions.com

(c) 2019. Axenic Health Solutions, Inc. All Rights Reserved

XX fl oz (XX mL) NDC: 73259-001-XX

INGREDIENTS AND APPEARANCE

Q SHIELD 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73259-001
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
DIMETHYLOCTADECYL(3-(TRIMETHOXYSILYL)PROPYL)AMMONIUM CHLORIDE (UNII: IQ36O85WQ4)
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73259-001-01	550 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	10/15/2019
2	NDC: 73259-001-04	50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	10/15/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	10/15/2019

Labeler - Pierce Innovations, LLC (091560426)

Establishment
Name	Address	ID/FEI	Business Operations
Fill Tech USA, LLC		926433855	label(73259-001) , pack(73259-001) , repack(73259-001) , relabel(73259-001) , manufacture(73259-001)