Label: ALCOHOL PREP PADS- isopropyl alcohol, alcohol prep pads swab

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

Drug Label Information

Updated December 10, 2024

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  • Active ingredient

    Isopropyl Alcohol 70%

  • Purpose

    Antiseptic

  • Uses

    First aid to help reduce the risk of infection in minor cuts, scrapes, and burns.

  • Warnings

    For external use only. Flammable. Keep away from heat or flame.

    Stop use and ask a doctor

    if the condition persists or gets worse. Do not use longer than 1 week unless directed by a doctor.

    Do not use

    • in the eyes or apply over large areas of the body. In case of deep or puncture wounds, animal bites, or serious bums, consult a doctor.

    Keep out of reach of children.If accidentally swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Apply to skin as needed.
    • Discard after single use.
    • Children under 6 years of age should be supervised by an adult when using this product.
  • Other information

    • Store in a cool, dry place, between 15°-30°C(59°F-86°F).
    • Avoid freezing and excessive heat above 40°C(104°F).
  • Inactive ingredients

    Water

  • Questions?

    Call 1-800-910-6874

  • Alcohol Prep Pads

    Alcohol Prep Pad Label

  • INGREDIENTS AND APPEARANCE
    ALCOHOL PREP PADS 
    isopropyl alcohol, alcohol prep pads swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78691-026
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL0.26 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:78691-026-01200 in 1 BOX08/05/2024
    11 g in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00308/05/2024
    Labeler - QUEST USA CORP (079869689)
    Registrant - QUEST USA CORP (079869689)
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