MY-SHIELD SANITIZING- benzalkonium chloride soap

MY-SHIELD SANITIZING by

Drug Labeling and Warnings

MY-SHIELD SANITIZING by is a Otc medication manufactured, distributed, or labeled by Enviro Specialty Chemicals Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient:

Benzalkonium Chloride 0.10%

Purpose:

Antiseptic Hand Soap

Uses:

Hand wash to help reduce bacteria that potentially can cause disease
Helps to prevent cross-contamination by hand contact
Helps to prevent drying of skin  Recommended for repeat use 

Warnings:

For external use only
When using this product do not use in or near eyes
Stop use and ask doctor if irritation and redness develop

Keep out of reach of children,
If swallowed, seek medical attention or contact a Poison Control Center immediately.

Directions:

Wet hands and wrists with clean running water
Apply appropriate amount of product 
Lather & scrub hands, fingers, fingernails, cuticles & wrists thoroughly 
Rinse thoroughly with running water 
Dry hands completely (incomplete drying may result in chapped skin)

Inactive Ingredients:

Aloe Barbadensis Leaf Juice, Aqua, Benzyl Alcohol, Citric Acid, Glycerin, Lauramidopropyl Betaine, Phenoxyethanol, Triethoxysilylpropyl Steardimonium Chloride.

Questions?

+1(888) 331-8332, M-F 9AM-5PM (EST)

SPL UNCLASSIFIED SECTION

KILLS 99.99% OF GERMS

Alcohol-Free

FDA Registered Anti-Microbial Soap for cleaning grime and germs from your hands

Formulated and enhanced with Zetrisil®

FAST ACTING 15 SECOND FORMULA

WITH SOOTHING ALOE VERA

FORMULATED IN THE USA | MADE IN CHINA

Store in a cool dry place below 104°F (40°C)

Distributed by: ESC Brands, LLC.

1060 Blue Prince Road

Bluefield, WV 24701

www.my-shield.com

Packaging

INGREDIENTS AND APPEARANCE

MY-SHIELD SANITIZING 
benzalkonium chloride soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71884-040
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
WATER (UNII: 059QF0KO0R)
BENZYL ALCOHOL (UNII: LKG8494WBH)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
GLYCERIN (UNII: PDC6A3C0OX)
LAURAMIDOPROPYL BETAINE (UNII: 23D6XVI233)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
TRIETHOXYSILYLPROPYL STEARDIMONIUM CHLORIDE (UNII: XGN40YQC7B)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71884-040-01	244 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2018
2	NDC: 71884-040-02	473 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2018
3	NDC: 71884-040-03	946 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2018
4	NDC: 71884-040-04	1182 mL in 1 BAG; Type 0: Not a Combination Product	05/01/2018
5	NDC: 71884-040-05	3785 mL in 1 PAIL; Type 0: Not a Combination Product	05/01/2018
6	NDC: 71884-040-06	18927 mL in 1 PAIL; Type 0: Not a Combination Product	05/01/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	05/01/2018

Labeler - Enviro Specialty Chemicals Inc (202621850)