BZK CLEANSER

Manufacturer
Geri-Gentle Corporation
Effective date
2025-10-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:39:28

Label at a glance#

ProductBZK CLEANSER
Active ingredientBENZALKONIUM CHLORIDE
Label structure13 sections

Indications and 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.

Dosage and administration

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

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1% w/w

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • 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

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

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

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • deep or punctured wonds
  • animal bites
  • serious burns

When using this product

OTC - WHEN USING SECTION

  • use only as directed
  • avoid contact with eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • 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

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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

OTHER SAFETY INFORMATION

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

Inactive Ingredients

INACTIVE INGREDIENT SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Drug FactDrug Fact

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130648289041279GTIN-13: 0648289041279
EAN-13: 0648289041279
GTIN-12: 648289041279
UPC-A: 648289041279
GTIN storage (14 digits): 00648289041279
GG-Wound Cleanser.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69771-062-01BZK CLEANSER237 g in 1 BOTTLE, PLASTICSOLUTION2371

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69771-06269771-062-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
BZK CLEANSERBENZALKONIUM CHLORIDEGeri-Gentle Corporation415eb5fb-5f88-d2dd-e063-6394a90abe5d2025-10-17WarningsExact identifier
ndc (package): 69771-062-01
ndc (product): 69771-062
ndc11 (package): 69771006201
spl id: 415eb5fb-5f89-d2dd-e063-6394a90abe5d
spl set id: 415eb5fb-5f88-d2dd-e063-6394a90abe5d

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.