Label: ISOPROPYL ALCOHOL- isopropyl alcohol spray spray

  • NDC Code(s): 67777-011-01, 67777-011-02
  • Packager: Dynarex Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 15, 2024

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  • Active Ingredient

    Isopropyl Alcohol 70%

  • Purpose

    First Aid Antiseptic

  • Use(s)

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

  • Warnings

    For External Use Only

    Do not use

    • Near eyes or mucous membranes • Over large areas of the body • Longer than 1 week unless directed by a doctor • With electrocautery procedures

    Ask a doctor before use if you have

    Deep or puncture wounds, animal bites, or serious burns.

    Stop use and ask a doctor if

    Condition persists for more than 72 hours or get worse.

    Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

  • Directions

    • Clean the affected area and spray 1 to 3 times daily • May be covered with a sterile bandage • If bandaged, let dry first

    • Children under 12 years of age: Consult a doctor before use

  • Other Information

    • Store at 20º-25ºC

    • Avoid excessive heat

  • Inactive Ingredient

    Purified Water

  • Questions?

    1-888-Dynarex Monday - Friday, 9AM - 5PM EST

  • Label 1166

    1166_IN_MASTERIsopropyl Alcohol Spray

  • INGREDIENTS AND APPEARANCE
    ISOPROPYL ALCOHOL 
    isopropyl alcohol spray spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-011
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    Color    Score    
    ShapeFREEFORMSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67777-011-0124 in 1 CASE02/29/2024
    1NDC:67777-011-0259.1 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00302/29/2024
    Labeler - Dynarex Corporation (008124539)
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