ELIMISHIELD HUNT CORE BODY FOAM FOR HUNTERS- benzalkonium chloride aerosol, foam

ElimiShield Hunt Core Body Foam for Hunters by

Drug Labeling and Warnings

ElimiShield Hunt Core Body Foam for Hunters by is a Otc medication manufactured, distributed, or labeled by Bryson Industries, Inc., Filltech USA, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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 iirtation develops 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 throughout body.
• Rub into skin until dry.

Inactive Ingredients

Aloe Barbadensis Leaf Juice extract.Caprylyl Glucoside, Citric Acid, Glycerin, Laureth-4, 1-Octadecanaminium NN Dimethyl (3-Trimethoxysilyl) Propyl Chloride, Phenoxyethanol, Polyaminopropyl biguanide, Water.

Package Labeling:

INGREDIENTS AND APPEARANCE

ELIMISHIELD HUNT CORE BODY FOAM FOR HUNTERS 
benzalkonium chloride aerosol, foam

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71853-010
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)
CAPRYLYL GLUCOSIDE (UNII: V109WUT6RL)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
GLYCERIN (UNII: PDC6A3C0OX)
LAURETH-4 (UNII: 6HQ855798J)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
POLYAMINOPROPYL BIGUANIDE (UNII: DT9D8Z79ET)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71853-010-00	200 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	505G(a)(3)	05/01/2020

Labeler - Bryson Industries, Inc. (040363256)

Establishment
Name	Address	ID/FEI	Business Operations
Filltech USA, LLC		926433855	manufacture(71853-010)