MEDICHOICE CLEANSING TOWELETTE- benzalkonium chloride liquid 
Owens & Minor Inc.

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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MediChoice Cleansing Towelette

MediChoice Cleansing Towelette


Active Ingredient

Benzalkonium Chloride, 0.13%

Purpose

First Aid Antiseptic

Use

First aid antiseptic product to apply topically to the skin to help prevent infection in minor cuts, scrapes, and burns.

Warnings

For external use only.

Do not use

■ in the eyes or apply over large areas of the body.

■ longer than 1 week unless directed by a doctor.

■ on infants Consult a doctor

■ in case of deep or puncture wounds, animal bites, or serious burns.

Stop use and consult a doctor

  • if the condition persists or gets worse

Keep out of reach of children.

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

Directions

■Clean the affected area 1 to 3 times daily or as directed by a doctor.

■ May be covered with a sterile bandage when dry.

Inactive Ingredients

Isopropyl Alcohol, Purified Water, Sodium Bicarbonate

MediChoice Cleansing Towelette 100 Count (39892-0302-1)

NDC 39892-0302-1

MEDICHOICE

Cleansing Towelette

Benzalkonium Chloride First Aid Antiseptic

For External use only.

CAUTION: Sterility of contents guaranteed in

unopened, undamaged package.

Not Made with natural latex

sterile

1/Each

Reorder:CLT100

Distributed by Owens & Minor

9120 Lockwood Boulevard

Mechanicsville, VA 23116

Made in China

CleansingTowelette

MEDICHOICE CLEANSING TOWELETTE 
benzalkonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:39892-0302
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 mg  in 100 mg
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:39892-0302-1100 in 1 BOX11/11/201406/16/2020
11600 mg in 1 PATCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A11/11/201406/16/2020
Labeler - Owens & Minor Inc. (847412269)
Registrant - Owens & Minor, Inc (847412269)

Revised: 1/2020
Document Id: 9c468220-f557-9eea-e053-2995a90a6bc6
Set id: 61cd9a0d-2bdf-4e53-92b0-a6fa5cadee05
Version: 4
Effective Time: 20200116
 
Owens & Minor Inc.