BZK SANITIZING HAND WIPES- benzalkonium chloride cloth 
Premium PPE, LLC

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.

----------

BZK Sanitizing Hand Wipes

Directions for Use:

Wipe liberally over the hands, rub into skin until dry. Recommended for single use.

Active Ingredient:

Benzalkonium Chloride 0.13%

Purpose:

Antiseptic/ hand and skin sanitizer

Uses:

Sanitizing hand wipes help decrease bacteria on the skin. Recommended for single use

Inactive Ingredients:

Aloe Barbadensis leaf extract, Aqua, Citric Acid, Caprylyl Glucoside, L a u r e t h - 4 , P o l y h e x a n i d e , Phenoxyethanol, Trielhoxysilylpropyl
Steardimonium Chloride.

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.

Questions?

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

Package Labeling:

Bottle6

BZK SANITIZING HAND WIPES 
benzalkonium chloride cloth
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81529-003
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:81529-003-0180 in 1 CANISTER02/03/2020
16.25 mL in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333E02/03/2020
Labeler - Premium PPE, LLC (117835683)

Revised: 2/2021
Document Id: bc2e9e3d-1eb8-027b-e053-2a95a90af076
Set id: bc2ea037-3dc3-5eca-e053-2a95a90a7f9d
Version: 1
Effective Time: 20210225
 
Premium PPE, LLC