ElimiShield Alcohol-Free Hand Sanitizer

ElimiShield Alcohol Free Hand Sanitizer by

Drug Labeling and Warnings

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

Drug Details [pdf]

ELIMISHIELD ALCOHOL FREE HAND SANITIZER- benzalkonium chloride liquid 
Bryson Industries Inc.

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ElimiShield Alcohol-Free Hand Sanitizer

Drug Facts

Active Ingredient

Benzalkonium chloride 0.13%

Purpose

Antiseptic Skin Sanitizer

Uses

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

Warnings

For external use only.

Do not use

in ears or mouth and avoid mucus membranes.

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

Water, Polyaminopropyl biguanide, 1-Octadecanaminium NN dimethyl (3-trimethoxysilyl) propyl chloride, Glycerin, Aloe Barbadenis Leaf Juice Extract, Caprylyl Glucoside, Citric Acid, DL Citronellol, Laureth-4, Phenoxyethanol,

Package Labeling:

ELIMISHIELD ALCOHOL FREE HAND SANITIZER 
benzalkonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71853-007
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
OCTADECYLDIMETHYL(3-TRIHYDROXYSILYLPROPYL)AMMONIUM CHLORIDE (UNII: GLJ50K866T)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GLYCERIN (UNII: PDC6A3C0OX)
.BETA.-CITRONELLOL, (+/-)- (UNII: 565OK72VNF)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYAMINOPROPYL BIGUANIDE (UNII: DT9D8Z79ET)
WATER (UNII: 059QF0KO0R)
CAPRYLYL GLUCOSIDE (UNII: V109WUT6RL)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
LAURETH-4 (UNII: 6HQ855798J)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71853-007-01	500 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/01/2020	12/31/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	09/01/2020	12/31/2024

Labeler - Bryson Industries Inc. (040363256)

Revised: 1/2025

Document Id: 2cd7e775-3c24-7a8e-e063-6394a90a6626

34390-5

Set id: b0002a22-118e-0ef9-e053-2a95a90ac1c2

Version: 3

Effective Time: 20250129