BZK CLEANSER- benzalkonium chloride solution

BZK CLEANSER by

Drug Labeling and Warnings

BZK CLEANSER by is a Otc medication manufactured, distributed, or labeled by Geri-Gentle Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Benzalkonium Chloride 0.1% w/w

Purpose

Antiseptic

Uses

• helps cleanse and protect skin and support healing of minor cuts, scrapes, burns and wounds.
• Topical antiseptic-to hel decrease the risk of infection.

For External Use Only

For external use only

Do not use

• in large quantities, particularly over raw surfaces or blistered areas

Ask a doctor before use if you have

• deep or punctured wonds
• animal bites
• serious burns

When using this product

• use only as directed
• avoid contact with eyes

Stop use and ask a doctor if

• condition persists or get worse, symptoms persist for more than 7 days or clear up and occur again witin few days

Keep out of reach of children

if swallowed, get medical help or contact Poisn Control Center immediately

Directions

• Adults and children 2 years of age and older
• use the spray to clean cuts, scrapes, wounds and burns by thoroghly flushing the affected area
• let dry
• cover with adhesive bandage or sterile gauze
• apply a small amount of this product on the area 1or 2 times daily
• for children under 2 years of age,consult a doctor

other information

• Keep container close when not in use
• Store at room temprature 68 -77 F (20-25 C)

Inactive Ingredients

Water, Disodium EDTA, Disodium Cocoamphodiacetate, DMDM Hydantoin, Imidazolidinyl Urea, Lactic Acid, Lauryl Polyglucose, Polysorbate 80, Triethanolamine, Sorbitol

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BZK CLEANSER 
benzalkonium chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69771-062
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
EDETATE DISODIUM (UNII: 7FLD91C86K)
LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
DMDM HYDANTOIN (UNII: BYR0546TOW)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
IMIDAZOLIDINYL UREA (UNII: M629807ATL)
LACTIC ACID, L- (UNII: F9S9FFU82N)
TRIETHANOLAMINE (UNII: 9O3K93S3TK)
SORBITOL (UNII: 506T60A25R)
DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69771-062-01	237 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/17/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	10/17/2025

Labeler - Geri-Gentle Corporation (080367686)