BZK ANTISEPTIC TOWELETTE- benzalkonium chloride solution

BZK Antiseptic Towelette by

Drug Labeling and Warnings

BZK Antiseptic Towelette by is a Otc medication manufactured, distributed, or labeled by H and P Industries, Inc. dba Triad Group. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Benzalkonium chloride .13% w/v

PURPOSE

Antiseptic

USE

First aid antiseptic to help prevent the risk of infection in minor cuts, scrapes and burns

WARNINGS

For external use only.

Do not

• use in the eyes
• apply over large areas of the body
• allow children to use except under adult supervision
  

Ask a doctor in case of

• deep or puncture wounds
• animal bites
• serious burns
  

Stop use and ask a doctor

if condition persists or gets worse

Keep out of reach of children

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

DIRECTIONS

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

SPL UNCLASSIFIED SECTION

STORAGE AND HANDLING

INACTIVE INGREDIENTS

fragrance, isopropyl alcohol, propylene glycol, sodium bicarbonate, water

QUESTIONS

CARTON INFORMATION

TRIAD

Cat. No. 10-5101
NDC: 50730-5101-0

ANTISEPTIC
TOWELETTES
with BENZALKONIUM CHLORIDE

A Soothing Pre-Moistened Antiseptic Towelette for Face and Hands
Cleans and Cools Simultaneously

100 towelettes

INGREDIENTS AND APPEARANCE

BZK ANTISEPTIC TOWELETTE 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 50730-5101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
benzalkonium chloride (UNII: F5UM2KM3W7) (benzalkonium - UNII:7N6JUD5X6Y)	benzalkonium chloride	.0013 mL

Inactive Ingredients
Ingredient Name	Strength
isopropyl alcohol (UNII: ND2M416302)
propylene glycol (UNII: 6DC9Q167V3)
sodium bicarbonate (UNII: 8MDF5V39QO)
water (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 50730-5101-0	100 in 1 CARTON
1		1 in 1 PACKET

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	10/17/1997

Labeler - H and P Industries, Inc. dba Triad Group (050259597)

Registrant - H and P Industries, Inc. dba Triad Group (050259597)

Establishment
Name	Address	ID/FEI	Business Operations
H and P Industries, Inc. dba Triad Group		050259597	manufacture