BZK ALCOHOL FREE HAND SANITIZER- benzalkonium chloride spray

BZK Alcohol Free Hand Sanitizer by

Drug Labeling and Warnings

BZK Alcohol Free Hand Sanitizer by is a Otc medication manufactured, distributed, or labeled by Premium PPE, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredient:

Benzalkonium Chloride 0.13%

Purpose:

Hand & Skin Sanitizer

Uses:

BZK™ Alcohol Free Hand Sanitizer provides revolutionary protection in an alcohol-free formula. The scientifically-proven solution kills harmful germs, bacteria, and microbes, and gently soothes and softens skin with aloe vera. Recommended for repeated use.

Warnings:

Do not freeze

+ For external use only 

Do not use

+ in ears, eyes 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 develops and persists for more than 72 hours

Keep out of reach of children

+Children should be supervised when using this product.

Directions:

Apply liberally to the palms of the hands or areas of damaged skin. Rub into skin until dry. Recommended for repeated use.

Other Information:

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

Inactive Ingredients:

Aloe Barbadensis leaf extract, Aqua, Citric Acid, Caprylyl Glucoside, Laureth-4, Polyhexanide, Phenoxyethanol, Triethoxysilylpropyl Steardimonium Chloride.

Questions?

1-800-920-7650 Mon-Fri 10AM-4PM (EST)

Package Labeling:

INGREDIENTS AND APPEARANCE

BZK ALCOHOL FREE HAND SANITIZER 
benzalkonium chloride spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 81529-001
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)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
CAPRYLYL GLUCOSIDE (UNII: V109WUT6RL)
LAURETH-4 (UNII: 6HQ855798J)
POLIHEXANIDE (UNII: 322U039GMF)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
TRIETHOXYSILYLPROPYL STEARDIMONIUM CHLORIDE (UNII: XGN40YQC7B)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 81529-001-01	59 mL in 1 BOTTLE; Type 0: Not a Combination Product	02/03/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333E	02/03/2021

Labeler - Premium PPE, LLC (117835683)