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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1302 Cleansing Towelettes NDC 67777-244-01

Active Ingredient

Benzalkonium Chloride 0.13% v/v

Purpose

First Aid Antiseptic

Uses

• For perineal and maternity care throughout postpartum and whenever refreshing is needed.

Warnings

For external use only

Do not use

• In the eye

Stop use and ask a doctor if

• Irritation and redness develop

• If condition persists for 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.

Directions

• Unfold towel

• Cleanse the desired area

• Dispose of towlette after single use.

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

Chlorothymol, Isopropyl Acohol, Water, may contain Methylchloroisothiazolinone/Methylisothiazolinone

Label

1302 BX MASTER1302 Label

Label

1302 MNFL0101302 Obstetrical Towelette

BZK PADS 
benzalkonium chloride swab
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-244
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
METHYLCHLOROISOTHIAZOLINONE/METHYLISOTHIAZOLINONE MIXTURE (UNII: 15O9QS218W)  
CHLOROTHYMOL (UNII: LJ25TI0CVT)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:67777-244-0110 in 1 CASE04/05/2011
1NDC:67777-244-02100 in 1 BOX
10.55 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: ee9d1fcf-3c8c-32c8-e053-2a95a90aed5a
Set id: 10454042-ff2e-44ce-b2e2-436cc004897f
Version: 21
Effective Time: 20221129
 
Dynarex Corporation