BZK TOWELETTE- benzalkonium chloride swab 
Dukal LLC

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65517-0004 - BZK

Drug Facts

Active Ingredients

Benzalkonium Chloride, 0.133% w/v

Use

First Aid to help reduce the risk of infection in minor cuts, scrapes and burns.

Purpose

First Aid Antiseptic

Do Not Use

In the eyes or apply over large areas of the body.

Stop Use

If irritation, redness or other symptoms develop. Consult a doctor if the condition persists or gets worse.

Caution

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Tear open packet, unfold and use as a washcloth.

Inactive Ingredients

Sodium Bicarbonate, Water

Principal Display Panel - 1.4 mL Pouch Label

Dukal
BZK ANTISEPTIC

TOWELETTE

Contains Benzalkonium Chloride / For External Use Only

Not made with natural rubber latex / Single Use

Manufactured For: Dukal, LLC

1(800)243-0741 / Ronkonkoma, NY 11779 / dukal.com

Made in China

Dukal is a trademark registered in the

US Patent & Trademark Office

by Dukal, LLC

1 Per Pack / NDC 65517-0004-1 REF 855

855

Principal Display Panel - 2.1 mL Pouch Label

Dukal
BZK ANTISEPTIC

TOWELETTE

Contains Benzalkonium Chloride / For External Use Only

Not made with natural rubber latex / Single Use

Manufactured For: Dukal, LLC

1(800)243-0741 / Ronkonkoma, NY 11779 / dukal.com

Made in China

Dukal is a trademark registered in the

US Patent & Trademark Office

by Dukal, LLC

1 Per Pack / NDC 65517-0004-2 / REF 855C

855C

BZK TOWELETTE 
benzalkonium chloride swab
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65517-0004
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
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:65517-0004-11.4 mL in 1 POUCH; Type 0: Not a Combination Product01/01/2006
2NDC:65517-0004-22.1 mL in 1 POUCH; Type 0: Not a Combination Product01/01/2006
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00301/01/2006
Labeler - Dukal LLC (791014871)

Revised: 3/2024
Document Id: 12649ebb-806d-bdea-e063-6394a90ac6d6
Set id: e37022d4-3d72-4d84-bddd-6b304fa0291e
Version: 16
Effective Time: 20240321
 
Dukal LLC