Label: ANTISEPTIC- antiseptic spray spray

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated October 14, 2021

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

  • Active Ingredients

    Benzalkonium Chloride 0.1%

    Benzocaine 5.0%

  • Purpose

    First aid antiseptic

    Topical pain relief

  • Uses

    First aid to help prevent infection and for temporary pain relief in minor cuts and burns

  • Warnings

    For external use only. Flammable keep away from fire or flame.

  • Flamable, keep away from fire or flame

  • Do Not Use

    • near eyes or mucous membranes
    • on deep or puncture wounds, animal bites or serious burns
    • over lare areas of the body
    • more than one week unless directed by a doctor
  • Keep out of reach of children.

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

  • Stop use and ask a doctor

    if condition persists or gets worse

  • Directions

    • clean the affected area and spray 1 to 3 times daily
    • may be covered with a sterile bandage
    • childern under 2 ask a doctor
  • Inactive ingredient

    Isopropyl alcohol, purified water

  • RapidCare - Antiseptic Spray - 2fl oz

    Antiseptic Spray

  • INGREDIENTS AND APPEARANCE
    ANTISEPTIC 
    antiseptic spray spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73659-011
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.001 mg
    BENZOCAINE (UNII: U3RSY48JW5) (BENZOCAINE - UNII:U3RSY48JW5) BENZOCAINE0.05 mg
    Inactive Ingredients
    Ingredient NameStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73659-011-021 in 1 BOTTLE; Type 0: Not a Combination Product12/15/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A12/15/2020
    Labeler - Rapid Care, Inc (877432778)