BZK PADS- benzalkonium chloride swab 
Dynarex Corporation

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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1301 Cleansing Towelettes NDC 67777-243-01

Active Ingredient

Benzalkonium Chloride 0.13% v/v

Purpose

First Aid Antiseptic

Uses

• First aid to help prevent skin infection in minor cuts, scrapes, and burns.

• Cleans and refreshes hand, face, and body without soap and water.

Warnings

For external use only

Do not use

• As an antiseptic for more than 1 week

• In the eyes

Ask a doctor before use if

you have deep or puncture wounds, animal bites, or serious burns.

Stop use and ask a doctor if

• Irritation and redness develop

• Condition persists or gets worse

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Direction

• Clean the affected area.

• May be covered with a sterile bandage

• If bandaged, let dry first

Other Information

• Store at room temperature 15º-30ºC (59º-86ºF).

• Avoid excessive heat.

• Tamper evident. Do not use if packet is torn or cut.

Inactive ingredients

Isopropyl Alcohol, Water, may contain Methylchloroisothiazolinone/Methylisothiazolinone

Questions?

1-888-Dynarex Monday - Friday, 9AM - 5PM EST

Label

1301 BX MASTER1301 Cleansing Towelettes

Label

1301 BX MNFL0101301 Cleansing Towelettes

BZK PADS 
benzalkonium chloride swab
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-243
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
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
WATER (UNII: 059QF0KO0R)  
METHYLCHLOROISOTHIAZOLINONE/METHYLISOTHIAZOLINONE MIXTURE (UNII: 15O9QS218W)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:67777-243-031000 in 1 CASE04/05/2011
1NDC:67777-243-02100 in 1 BOX
1NDC:67777-243-010.55 mL in 1 PACKET; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A04/05/2011
Labeler - Dynarex Corporation (008124539)
Registrant - Dynarex Corporation (008124539)

Revised: 11/2022
Document Id: ee9d9d31-55c4-5f56-e053-2995a90a7f8b
Set id: 87288939-cc34-4437-94ab-dcb997d6acd5
Version: 28
Effective Time: 20221129
 
Dynarex Corporation