Label: FIRST SHIELD FIRST AID ANTISEPTIC- benzalkonium chloride spray

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 15, 2024

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

View All Sections
  • ACTIVE INGREDIENT

    Active ingredient

    Benzalkonium chloride 0.13%

  • PURPOSE

    Purpose

    First aid antiseptic

  • INDICATIONS & USAGE

    Uses

    First aid to help prevent infection in minor cuts, scrapes & burns

  • WARNINGS

    Warnings

    For external use only

    Flammable keep away from fire or flame

  • DO NOT USE

    Do not use* near eyes or mucous membranes *on deep or puncture wounds , animal bites, or serious burns *over large areas of the body* more than one week unless directed by a doctor

  • STOP USE

    Stop use and ask a doctor if condition persists or gets worse

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Directions

    • clean affected area & spray 1 to 3 times daily
    • may be covered with a sterile bandage
    • not to be used on children under 12 of years of age.
  • INACTIVE INGREDIENT

    Inactive ingredients ethyl alcohol, purified water

  • QUESTIONS

    Questions or comments？ 800-325-4655

  • PRINCIPAL DISPLAY PANEL

    image of bottle label

  • INGREDIENTS AND APPEARANCE
    FIRST SHIELD FIRST AID ANTISEPTIC 
    benzalkonium chloride spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72976-003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72976-003-0160 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product05/30/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00305/30/2022
    Labeler - Ever Ready First Aid (147372960)
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!