MICROKLENZ ANTIMICROBIAL- benzethonium chloride liquid 
Medline Industries, LP

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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073 MicroKlenz First Aid Antiseptic

Active ingredient

Benzethonium Chloride 0.1%

Purpose

First Aid Antiseptic

Uses

For first aid to help prevent infection in:

Warnings

For external use only. Avoid contact with eyes.

Ask a doctor before use if you have

  • deep or puncture wounds
  • animal bites
  • serious burns

When using this product

  • do not use in or near the eyes
  • do not apply over large areas of the body or in large quantities
  • do not use longer than 1 week unless directed by a doctor

Stop use and ask a doctor if

  • condition worsen or if symptoms persist for more than 7 days or clear up and occur again within a few days.

Keep out of reach of children.

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

Directions

Inactive ingredients

citric acid, cocamidopropyl betaine, disodium phosphate, phenoxyethanol, water

Manufacturing Information

Manufactured for:

Medline Industries, LP

Three Lakes Drive, Northfield, IL 60093 USA

Made in the USA with foreign and domestic materials

www.medline.com

1-800-MEDLINE (633-5463)

REF: CRR108008

V2 RG22SAP

Package Label

Label V2 RG22SAP

MICROKLENZ ANTIMICROBIAL 
benzethonium chloride liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53329-073
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP) BENZETHONIUM CHLORIDE0.1 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:53329-073-08236 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product01/01/2007
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/01/2007
Labeler - Medline Industries, LP (025460908)
Registrant - Medline Industries, LP (025460908)

Revised: 7/2022
Document Id: e9ac358e-c9bf-7091-e053-2a95a90a4609
Set id: 115dda08-709c-490a-9693-419b51441960
Version: 6
Effective Time: 20220731
 
Medline Industries, LP