MICROKLENZ ANTIMICROBIAL- benzethonium chloride liquid

MicroKlenz Antimicrobial by

Drug Labeling and Warnings

MicroKlenz Antimicrobial by is a Otc medication manufactured, distributed, or labeled by Medline Industries, LP. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Benzethonium Chloride 0.1%

Purpose

First Aid Antiseptic

Use

for first aid to help prevent infection in

• minor cuts
• scrapes
• burns

Warnings

For external use only.

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 worsens
• 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

• Clean affected area
• Adjust nozzle and spray a small amount of this product on the area 1 to 3 times daily
• If used as a wet compress, keep bandage wet with solution
• If covered with a sterile bandage, let dry first.

Inactive ingredients

Citric Acid, Cocamidopropyl Betaine, Disodium Phosphate, Phenoxyethanol, Water.

Principal Display Panel

NDC: 53329-073-08

MEDLINE CARRINGTON

MicroKlenz

ANTIMICROBIAL

FIRST AID ANTISEPTIC

REF CRR108008

An antimicrobial solution with wetting agents and surfactants uniquely blended to help decrease the risk of infection.

PROTECT AGAINST BACTERIAL CONTAMINATION

8 FL OZ (236 mL)

INGREDIENTS AND APPEARANCE

MICROKLENZ ANTIMICROBIAL 
benzethonium chloride liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53329-073
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZETHONIUM CHLORIDE (UNII: PH41D05744) (BENZETHONIUM - UNII:1VU15B70BP)	BENZETHONIUM CHLORIDE	0.1 mg  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53329-073-08	236 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	01/01/2007

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/01/2007

Labeler - Medline Industries, Inc. (025460908)

Establishment
Name	Address	ID/FEI	Business Operations
3001451826		080170933	manufacture(53329-073)