UEC MEDICAL BZK ANTISEPTIC WIPES- benzalkonium chloride cloth

UEC Medical BZK Antiseptic Wipes by

Drug Labeling and Warnings

UEC Medical BZK Antiseptic Wipes by is a Otc medication manufactured, distributed, or labeled by United Exchange Corp.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredient                                            Purpose

Benzalkonium Chloride 0.13% v/v....................Antiseptic

PURPOSE

Use

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

WARNINGS

Warnings For external use only.

DO NOT USE

Do not use

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

ASK DOCTOR

Ask a doctor before use if you have

• deep or puncture wounds
• animal bites
• serious burns

STOP USE

Stop use and ask a doctor

• if irritation and redness develops
• if condition persists for more than 72 hours

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

INDICATIONS & USAGE

Directions

• clean the affected area
• apply a small amount of this product on the area 1 to 3 times daily
• may be covered with sterile bandage
• if bandaged let dry first

INACTIVE INGREDIENT

Inactive ingredient purified water

DOSAGE & ADMINISTRATION

Manufactured exclusively for:

UEC Medical Co.

17211 Valley View Ave.

Cerritos, CA 90703 USA

www.uecmedical.com

PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

UEC MEDICAL BZK ANTISEPTIC WIPES 
benzalkonium chloride cloth

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 65923-345
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.13 g  in 100 g

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 65923-345-25	25 in 1 BOX	03/10/2017
1		3 g in 1 POUCH; Type 0: Not a Combination Product
2	NDC: 65923-345-10	100 in 1 BOX	03/10/2017
2		3 g in 1 POUCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	02/19/2016

Labeler - United Exchange Corp. (840130579)