MY-SHIELD SANITIZING- benzalkonium chloride liquid

My-Shield Sanitizing by

Drug Labeling and Warnings

My-Shield Sanitizing by is a Otc medication manufactured, distributed, or labeled by ESC Brands LLC, Filltech USA, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient:

Benzalkonium Chloride 0.13%

Purpose:

Antiseptic Hand Soap

Uses

Handwash to help reduce bacteria that potentially can cause disease Helps to prevent crosscontamination 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 and scrub hands, fingers, fingernails, cuticles and wrists thoroughly Rinse thoroughly with running water  Dry hands completely (incomplete drying may result in chapped skin)

Other Information

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

Inactive ingredients

Aloe Barbadensis Leaf Juice, Aqua, Benzyl Alcohol, Citric Acid, Glycerin, Hydrolysed Silk, Lauramidopropyl Betaine, Phenoxyethanol.

Questions?

+1 (336) 655 2219 Mon-Fri 9:00AM-5:00PM (EST)

Package Labeling:

INGREDIENTS AND APPEARANCE

MY-SHIELD SANITIZING 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71884-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 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)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71884-003-08	250 mL in 1 BOTTLE; 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 not final	part333E	05/01/2018

Labeler - ESC Brands LLC (202621850)

Establishment
Name	Address	ID/FEI	Business Operations
Filltech USA, LLC		926433855	manufacture(71884-003)