Label: ISOPROPYL RUBBING ALCOHOL- isopropyl alcohol solution

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated October 7, 2020

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  • Drug Facts

  • Active Ingredient

    Isopropyl Alcohol 91% 

  • 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

    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 ot apply over large areas of the body

    ● do not use longer than 1 week unless directed by a doctor

  • STOP USE

    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 a small amount of this product 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

  • PRINCIPAL DISPLAY PANEL

    TAMPER EVIDENT CAP FOR YOUR PROTECTION. IF RING-BAND IS DETACHED FROM CAP OR MISSING DO NOT USE.

    Part # HSN2237

    NDC #87010-004-32

    Isopropyl Rubbing Alcohol 91%

    FIRST AID ANTISEPTIC

    Isopropyl Alcohol

    Manufactured for Healthwell

    32 FL OZ

    (946 mL)

    Isopropyl Alcohol

  • INGREDIENTS AND APPEARANCE
    ISOPROPYL RUBBING ALCOHOL 
    isopropyl alcohol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:87010-004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL91 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:87010-004-16473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/07/2018
    2NDC:87010-004-32946 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product12/07/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A12/07/2018
    Labeler - Healthwell (004227758)
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