CLEANSE- benzalkonium chloride solution 
Medline Industries, LP

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184 Antibacterial Foaming Hand Soap

Active ingredient

Benzalkonium chloride 0.13%

Purpose

Antibacterial

Use

for handwashing to decrease bacteria on the skin

Warnings

For external use only: hands only

When using this product

  • avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if

  • irritation or redness develops
  • condition persists for more than 72 hours

Keep out of reach of children.

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

Directions

Inactive ingredients

benzophenone-4, citric acid, cocamidopropyl betaine, fragrance, glycerin, lauramidopropylamine oxide, lauramine oxide, myristamidopropylamine oxide, red 4, sodium benzoate, tetrasodium EDTA, water, yellow 5

Manufacturing Information

Manufactured for:

Medline Industries, LP

Three Lakes Drive, Northfield, IL 60093 USA

Made in USA with domestic and foreign materials

www.medline.com

1-800-MEDLINE (633-5463)

REF: HHABSP1200F

V2 RG23VJO

Package Label

Front Label V2 RG23VJO

Back Label V2 RG23VJO

CLEANSE 
benzalkonium chloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53329-184
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
LAURAMINE OXIDE (UNII: 4F6FC4MI8W)  
EDETATE SODIUM (UNII: MP1J8420LU)  
GLYCERIN (UNII: PDC6A3C0OX)  
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
FD&C RED NO. 4 (UNII: X3W0AM1JLX)  
SULISOBENZONE (UNII: 1W6L629B4K)  
MYRISTAMIDOPROPYLAMINE OXIDE (UNII: 3HSF539C9T)  
LAURAMIDOPROPYLAMINE OXIDE (UNII: I6KX160QTV)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:53329-184-841000 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product09/26/2016
2NDC:53329-184-08221 mL in 1 BOTTLE; Type 0: Not a Combination Product01/01/2021
3NDC:53329-184-741200 mL in 1 BOTTLE; Type 0: Not a Combination Product08/01/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph Drug505G(a)(3)09/26/2016
Labeler - Medline Industries, LP (025460908)
Registrant - Medline Industries, LP (025460908)

Revised: 5/2024
Document Id: 199de43a-3aca-3b5e-e063-6394a90a7581
Set id: 428644dd-b2e5-1675-e054-00144ff88e88
Version: 9
Effective Time: 20240529
 
Medline Industries, LP