FDA.reportPublic FDA data

Sterile Antibacterial Wound Wash

Manufacturer
Cosrich Group, Inc. | BOV Solutions Inc
Effective date
2025-11-18
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
full-release
Hydrated at
2026-06-01 01:16:52

Label at a glance#

ProductSterile Antibacterial Wound Wash
Active ingredientBENZETHONIUM CHLORIDE
Label structure9 sections

Indications and uses

first aid to help prevent the risk of bacterial contamination in minor cuts, scrapes and burns.

Dosage and administration

clean the affected area shake well remove seal and cap spray a small amount of this product on the area 1 to 3 times a day may be covered with a sterile bandage. If bandaged, let dry first

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzethonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

First Aid Antiseptic

Uses

INDICATIONS & USAGE SECTION

first aid to help prevent the risk of bacterial contamination in minor cuts, scrapes and burns.

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • in eyes
  • over large areas of the body
  • longer than 1 week unless directed by a doctor

Ask a doctor before use

OTC - ASK DOCTOR SECTION

in the event of deep puncture wounds, animal bites or severe burns

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition persists or gets worse

Keep out of reach of childrens

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • clean the affected area
  • shake well
  • remove seal and cap
  • spray a small amount of this product on the area 1 to 3 times a day
  • may be covered with a sterile bandage. If bandaged, let dry first

Other information

SPL UNCLASSIFIED SECTION

Do not

  • puncture or incinerate can. Contents under pressure
  • drop can
  • store at temperatures above 120 oF.
  • use if tamper evident seal is broken

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Extract, benzalkonium chloride, Purified Water, Sodium Chloride U.S.P.

Questions?

OTC - QUESTIONS SECTION

1-800-831-7210 

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 71029-390-04

PRO+ECT

Antibacterial WOUND WASH

FIRST AID CLEANSER

  • Cleans wounds painlessly and effectively
  • No burn or sting
  • No alcohol
  • No fragrance

ECO-FRIENDLY

No Fluorinated Hydrocarbon Propellants



  • COMPRESSED AIR IS THE PROPELLANT
  • SPRAYS UPSIDE DOWN OR AT ANY ANGLE
  • NO PUMPING NEEDED

360 0 CONTINUOUS SPRAY

4 FL.OZ (120 mL)


Label
Label



DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582205benzethonium chloride 0.13 % Topical SprayPSN9
582205benzethonium chloride 1.3 MG/ML Topical SpraySCD9
582205benzethonium chloride 0.13 % Topical SpraySY9

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71029-390-042020-06-02C16284748780-19d75b9d0-d9a5-f424-e053-dadaa90a57ceDrug Facts
71029-390-042020-01-31C16284748780-19d75b9d0-d9a5-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71029-390-04Sterile Antibacterial Wound Wash120 mL in 1 CANSPRAY1209

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71029-39071029-390-04

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
SODIUM CHLORIDE451W47IQ8XIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7IACT
BENZETHONIUM CHLORIDEPH41D05744ACTIB

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
43e5d7ab-a84d-171b-e063-6394a90a311ad86d3988-ee4b-4396-8b5a-164c4f0394e62025-11-18WarningsExact identifier
spl id: 43e5d7ab-a84d-171b-e063-6394a90a311a
spl set id: d86d3988-ee4b-4396-8b5a-164c4f0394e6

Reported adverse events (FAERS/openFDA)#

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