Label: ISOPROPYL ALCOHOL spray

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

Drug Label Information

Updated April 26, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Isopropyl Alcohol 70%

  • 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

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

  • STOP USE

    Stop use and ask a doctor if conditions persist or get worse.

  • Directions

    • clean the affected area
    • apply a small amount of this product on the area 1 - 3 times daily
    • children under 2 ask a doctor
  • Other Information

    • store at room temperature
  • Inactive Ingredients

    purified water

  • Questions?

    1-866-651-3660

    Mon-Fri 8:00am-5:00pm EST

    Manufactured for American Safety & First Aid Osceola, IN 46561

  • Principal Display Panel – Bottle Label

    0651

    NDC 73598-0651-1

    Isopropyl
    Alcohol

    First Aid Antiseptic

    First Aid to Help
    Prevent Infection in
    Minor Cuts, Scrapes
    and Burns.

    American Safety
    & First Aid

    2 fl. Oz. (59.1 ml)

    Principal Display Panel – Bottle Label
  • INGREDIENTS AND APPEARANCE
    ISOPROPYL ALCOHOL 
    isopropyl alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73598-0651
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Isopropyl Alcohol (UNII: ND2M416302) (Isopropyl Alcohol - UNII:ND2M416302) Isopropyl Alcohol700 mL  in 1 L
    Inactive Ingredients
    Ingredient NameStrength
    water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73598-0651-10.0591 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product02/14/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph drugM00402/14/2020
    Labeler - JHK Inc (867236309)
    Registrant - Safetec of America, Inc. (874965262)
    Establishment
    NameAddressID/FEIBusiness Operations
    Safetec of America, Inc.874965262MANUFACTURE(73598-0651)
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