BZK ALCOHOL FREE HAND SANITIZER- benzalkonium chloride liquid 
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Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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BZK Alcohol Free Hand Sanitizer

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:150ml

Bottle4

Package Labeling:50ml

Label

Package Labeling:500ml

Label2

BZK ALCOHOL FREE HAND SANITIZER 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81529-002
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:81529-002-02150 mL in 1 BOTTLE; Type 0: Not a Combination Product02/03/2021
2NDC:81529-002-0150 mL in 1 BOTTLE; Type 0: Not a Combination Product02/03/2021
3NDC:81529-002-03500 mL in 1 BOTTLE; Type 0: Not a Combination Product02/03/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E02/03/2020
Labeler - Premium PPE, LLC (117835683)

Revised: 3/2021
Document Id: bd07a9e9-2a97-1cef-e053-2995a90a6cea
Set id: bd07aa82-c3b4-1da3-e053-2995a90a6b79
Version: 1
Effective Time: 20210308
 
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