ELIMISHIELD CLINICAL HAND SANTIZER- benzalkonium chloride liquid

ElimiShield Clinical Hand Santizer by

Drug Labeling and Warnings

ElimiShield Clinical Hand Santizer by is a Otc medication manufactured, distributed, or labeled by Bryson Industries Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient

Benzalkonium chloride 0.13%

Purpose

Antiseptic Hand Sanitizer

Uses

• Hand sanitizer to help decrease bacteria on the skin.
• Recommended for repeated use.

Warnings

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 a small amount into palms of hands and spread on both hands.
• Rub into skin until dry.

Inactive Ingredients

1-Octadecanaminium NN dimethyl (3-trimethoxysilyl) propyl chloride, 1-Octadecanaminium NN dimethyl (3-trihydroxysily) propyl chloride, Aloe Barbadenis leaf extract, Aqua, Caprylyl glucoside, Citric acid, Laureth-4, Methylparaben, Polyaminopropyl Biguanide, Silk protein

Package Labeling:

INGREDIENTS AND APPEARANCE

ELIMISHIELD CLINICAL HAND SANTIZER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71853-001
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: 71853-001-01	50 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/02/2017
2	NDC: 71853-001-07	207 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/02/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	11/02/2017

Labeler - Bryson Industries Inc. (040363256)