CUT CARE BENZALKONIUM CHLORIDE ANTISEPTIC- benzalkonium chloride swab

Cut Care Benzalkonium Chloride Antiseptic by

Drug Labeling and Warnings

Cut Care Benzalkonium Chloride Antiseptic by is a Otc medication manufactured, distributed, or labeled by Zeus Medical Holdings LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Active Ingredient

Benzalkonium Chloride 0.13% v/v

Purpose

Antiseptic

Uses

First aid antiseptic to help prevent skin infection in minor cuts, scrapes and burns

Warnings

For external use only.

Do not use

• as a first aid antiseptic for more than 1 week
  
• in the eyes
  
• over large areas of the body

Ask a doctor before use

• deep or puncture wounds
  
• animal bites
  
• serious burns

Stop use if

• irritation and redness develop
  
• if condition persists for more than 72 hours, consult a physician.

Keep out of reach of children

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

Directions

• clean affected area
  
• apply 1 to 3 times daily
  
• may be covered with a sterile bandage
  
• if bandaged let dry first

Inactive ingredient

purified water

PRINCIPAL DISPLAY PANEL

NDC: 53439-130-10
Cut Care
Benzalkonium Chloride Antiseptic Towelette
First aid antiseptic
Contents: 100 Towelettes

INGREDIENTS AND APPEARANCE

CUT CARE BENZALKONIUM CHLORIDE ANTISEPTIC 
benzalkonium chloride swab

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53439-130
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	1.3 mg

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53439-130-10	100 in 1 CARTON
1	NDC: 53439-130-01	1 in 1 POUCH

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part333A	09/15/2013

Labeler - Zeus Medical Holdings LLC (014884052)