Label: XPECT ISOPROPYL ALCOHOL- isopropyl alcohol spray

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

Drug Label Information

Updated December 28, 2023

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  • Active ingredients

    Isopropyl Alcohol 70.0%

  • Purpose

    First Aid Antiseptic

  • Uses

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

  • Warnings

    For external use only 

    Flammable keep away from fire or flame

  • DO NOT USE

    Do not use

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

    Ask a doctor before use if you have

    • deep or puncture wounds
    • animal bites
    • serious burns
  • 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.

  • Directions

    • clean the affected area
    • spray a small amount 1 to 3 times daily
    • may be covered with a sterile bandage. 
    • if bandaged, let dry first 
  • Other information

    • store at room temperature
  • Inactive Ingredients

    purified water 

  • Questions?

    1-877-973-2811 M-F 8am-5pm

  • Principal Display Panel

    Isopropyl Alcohol

    Rubbing Formula

    Convenient pump spray allows no-touch application. Use as a rubbing compound, an antiseptic, or as a cleaning disinfectant for instruments.

    2 fl. oz. (59.1 mL)

    Xpect® First aid

    Bottle

  • INGREDIENTS AND APPEARANCE
    XPECT ISOPROPYL ALCOHOL 
    isopropyl alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:42961-201
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:42961-201-0159.1 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product01/26/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00301/26/2022
    Labeler - Cintas Corp (056481716)
    Establishment
    NameAddressID/FEIBusiness Operations
    Safetec of America, Inc874965262manufacture(42961-201)
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