Label: HANDY SOLUTIONS RUBBING ALCOHOL- isopropyl alcohol liquid

  • NDC Code(s): 67751-002-01
  • Packager: Navajo Manufacturing Company Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 15, 2024

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  • Handy Solutions Rubbing Alcohol


  • Active ingredient

    Isopropyl alcohol 70%

    Purpose

    First Aid Antiseptic

  • Uses

    • first aid to help prevent the risk of infection in:
      • minor cuts
      • scrapes
      • burns
  • Warnings

    For external use only

    Flammable

    • keep away from fire or flame, heat, spark, electrical. Flash point 72°F

    • do not use

    with electrocautery procedures.

    Ask a doctor before use if you have

    deep or puncture wounds, animal bites or serious burns

    When using this product

    • do not get into eyes
    • do not apply over large areas of the body
    • do not use longer than 1 week unless directed by a doctor

    Stop use and ask a doctor if

    condition persists or gets worse

    Keep out of reach of children.

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

  • Directions

    • clean the affected area
    • apply 1 to 3 times daily
  • Other information

    • does not contain, nor is intended as a substitute for grain or ethyl alcohol
    • will produce serious gastric disturbances if taken internally
  • Inactive ingredient

    purified water

  • Handy Solutions

    is a Trademark of Navajo Mfg. Co. Inc
    5330 Fox 5t., Denver, CO 80216

  • PRINCIPAL DISPLAY PANEL

    Handy Solutions ISOPROPYL RUBBING ALCOHOL

    70% by volume

    First aid antiseptic

    Warning: Do not use if tamper evident seal is broken.  This product is sealed with a breakaway cap.

    4 FL OZ (118 ml)

    image description

  • INGREDIENTS AND APPEARANCE
    HANDY SOLUTIONS RUBBING ALCOHOL 
    isopropyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67751-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL700 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67751-002-01118 mL in 1 BOTTLE; Type 0: Not a Combination Product08/15/2013
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00308/15/2013
    Labeler - Navajo Manufacturing Company Inc. (091917799)
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