Label: ISOPROPYL ALCOHOL- alcohol spray

  • NDC Code(s): 42961-056-01, 42961-056-02
  • Packager: Cintas Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 28, 2023

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  • Active ingredient

    Isopropyl alcohol 70%

  • Purpose

    First aid antiseptic

  • Uses

    first aid to help prevent infection in minor

    • cuts
    • scrapes
    • burns
  • Warnings

    For external use only.

    Caution: FLAMMABLE. Keep away from fire, flame or heat

    Do not use

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

    Ask a doctor before use if you have a

    • deep wound
    • puncture wound
    • animal bite
    • serious burns

    Stop use and ask a doctor if

    • the condition persists or gets worse

    Keep out of the 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 of this product in the area 1 to 3 times daily
    • may be covered with a sterile bandage. If bandaged, let dry first
  • Other information

    • store at room temperature
    • this product is not made from ethyl or grain alcohol and it is not intended as a substitute
  • Inactive ingredient

    purified water

  • Questions?

    1-800-841-8417 or zeemedical.com

  • Principal Display Panel

    ISOPROPYL ALCOHOL SPRAY

    First Aid Antiseptic

    Treats minor cuts and scrapes

    Helps prevent infection

    2 fl oz (59 ml)

    ZEE

    Distributed by ZEE MEDICAL, INC.

    label-01

  • INGREDIENTS AND APPEARANCE
    ISOPROPYL ALCOHOL 
    alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:42961-056
    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:42961-056-0159 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product04/13/2021
    2NDC:42961-056-02118 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product04/13/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00304/13/2021
    Labeler - Cintas Corporation (056481716)
    Establishment
    NameAddressID/FEIBusiness Operations
    Water-Jel Technologies155522589manufacture(42961-056)
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