Label: ALCOHOL PREP PAD MEDIUM BULK- isopropyl alcohol swab

  • NDC Code(s): 53329-778-97
  • Packager: Medline Industries, Inc.
  • Category: HUMAN OTC DRUG LABEL

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 September 10, 2009

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  • Active ingredient

    Isopropyl Alcohol 70%

  • Purpose

    Antiseptic

  • Uses

    For preparation of the skin prior to injection. For first aid to decrease germs in minor cuts, scrapes and burns.

  • Warnings

    • For external use only.
    • Flammable.Keep away from fire or flame.
    • Use only in a well-ventilated area; fumes may be toxic.
  • Do not use

    • with electrocautery procedures
    • longer than 1 week unless directed by a doctor

  • When using this product do not

    • get into eyes
    • apply over large areas of the body
    In case of deep or puncture wounds, animal bites or serious burns, consult a doctor.
  • Stop use and ask a doctor if

    • condition persists or gets worse or lasts for more than 72 hours
  • Keep out of reach of children

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

  • Directions

    • Wipe injection site vigorously
    • Apply to skin as needed
    • Discard after single use
  • Storage

    Protect from freezing. Avoid excessive heat.

  • Inactive ingredient

    Water

  • Questions

    1-800-MEDLINE

  • Principal Display Panel

    Alcohol Prep Pads

    For external use only

    Image of Isopropyl Alcohol MDS090737.jpg

  • INGREDIENTS AND APPEARANCE
    ALCOHOL PREP PAD  MEDIUM BULK
    isopropyl alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:53329-778
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Isopropyl Alcohol (UNII: ND2M416302) (Isopropyl Alcohol - UNII:ND2M416302) Isopropyl Alcohol0.70 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:53329-778-973000 in 1 BOX
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart33301/01/2077
    Labeler - Medline Industries, Inc. (025460908)
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