Label: WOUND WASH ANTISEPTIC SALINE WITH BENZALKONIUM CHLORIDE aerosol, spray

  • NDC Code(s): 13709-235-11
  • Packager: NeilMed Pharmaceuticals, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 11, 2024

If you are a consumer or patient please visit this version.

View All Sections
  • Dosage and Administration

    Before use, spray a short stream in the air or on intact skin to test spray pattern and to clear nozzle.

    To dispense, aim nozzle at the affected area and spray from a distance of 2 to 4 inches, or as is comfortable.

    Cover with clear cap after each use

  • Warnings

    Do not use on burn injuries. Do not use in body orifices, ear canals, eyes or mouth.

    Not for injection.

    For individual use only.

    Apply as needed. Consult a healthcare professional for continued wound care management and for use on children younger than 2 years of age.

  • Inactive Ingredients

    USP Grade Water, USP Sodium Chloride (9mg/mL)

  • OTC Active Ingredient

    Benzalkonium Chloride 0.13%

  • Indications and Usage

    First Aid Antiseptic

    First aid to cleanse minor cuts, wounds and scrapes

  • OTC- Purpose

    First aid to cleanse minor cuts, wounds and scrapes

  • OTC- Keep Out of Reach of Children

    Keep out of reach of children.

  • Wound Wash Antiseptic Sterile Saline with Benzalkonium Chloride, 75 mL

    Wound Wash 75ml

  • INGREDIENTS AND APPEARANCE
    WOUND WASH ANTISEPTIC SALINE WITH BENZALKONIUM CHLORIDE 
    wound wash antiseptic saline with benzalkonium chloride aerosol, spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:13709-235
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE1.3 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM CHLORIDE (UNII: 451W47IQ8X) 9 mg  in 1 mL
    WATER (UNII: 059QF0KO0R) 89.7 mg  in 1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:13709-235-1175 mL in 1 CAN; Type 0: Not a Combination Product01/02/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00401/02/2017
    Labeler - NeilMed Pharmaceuticals, Inc. (799295915)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!