MY-SHIELD TOPICAL ANTISEPTIC- benzalkonium chloride liquid

My-Shield Topical Antiseptic by

Drug Labeling and Warnings

My-Shield Topical Antiseptic 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 0.13%

Purpose

First aid antiseptic - Topical skin treatment

Uses

• First aid soothing and germ protection for: minor cuts abrasions  pressure sores sunburn scrapes burns skin irritations

Warnings

Do not freeze. For external use only.

Do not use 

in ears or mouth.

When using this product,

• avoid contact with the eyes. In case of contact flush eyes with water.

Stop use and ask a doctor if

redness or irritation develop and persist for more than 72 hours.

Keep out of reach of children.

Children should be supervised when using this product.

Directions

Apply liberally over effected area, recommended for repeat application regularly.

Inactive Ingredients

1-Octadecanaminium NN dimethyl (3-trimethoxysilyl) propyl chloride, 1-Octadecanaminium NN dimethyl (3-trihydroxysilyl) propyl chloride, Aloe Barbadenis leaf extract, Aqua, Caprylyl Glucoside, Citric Acid, Hydroxyethyl cellulose, laureth-4, Methyl Parabens, Polyaminopropyl biguanide, Silk Protein.

Questions?

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

Package Labeling:

INGREDIENTS AND APPEARANCE

MY-SHIELD TOPICAL ANTISEPTIC 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71884-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	13 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CAPRYLYL GLUCOSIDE (UNII: V109WUT6RL)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
LAURETH-4 (UNII: 6HQ855798J)
METHYLPARABEN (UNII: A2I8C7HI9T)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71884-001-02	57 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2017
2	NDC: 71884-001-04	118 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2017
3	NDC: 71884-001-06	177 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/15/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	11/15/2017

Labeler - Enviro Specialty Chemicals Inc (202621850)