Label: ALCOHOL WIPE- isopropyl alcohol swab
ALCOHOL PREP PAD- isopropyl alcohol swab

  • NDC Code(s): 0498-0142-34, 0498-0143-04, 0498-0143-05, 0498-0143-10, view more
    0498-0143-33, 0498-0143-34
  • Packager: Honeywell Safety Products USA, Inc
  • Category: HUMAN OTC DRUG LABEL

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Drug Label Information

Updated January 12, 2024

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  • 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 and flame

    Do not use

    • in or near eyes
    • over large areas of the body

    Ask a doctor before use if you have

    • deep or puncture wounds
    • animal bites
    • serious burns

    When using this product

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

    Stop use and consult a doctor if

    • condition persists or gets worse

    Keep out of the reach of children

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

  • Directions

    • clean the affected area
    • may be covered with a sterile bandage
    • apply wipe to affeted are 1 to 3 times daily
    • discard wipe after single use
  • Other information

    • store at room temperature 15 o to 25 o C (59 o to 77 oF)
    • do not use if packet is torn or opened
  • Inactive ingredient

    water

  • Questions

    1-800-430-5490

  • alcohol wipes

    Alcool wipes

  • Alcohol wipes 10 ct

    Alcool wipes 10

  • OH Pak

    OH pak

  • INGREDIENTS AND APPEARANCE
    ALCOHOL WIPE 
    isopropyl alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0498-0143
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0498-0143-040.4 mL in 1 POUCH; Type 0: Not a Combination Product09/18/2018
    2NDC:0498-0143-3410 in 1 BOX09/18/2018
    20.4 mL in 1 POUCH; Type 0: Not a Combination Product
    3NDC:0498-0143-0550 in 1 BOX09/18/2018
    30.4 mL in 1 POUCH; Type 0: Not a Combination Product
    4NDC:0498-0143-10100 in 1 BOX09/18/2018
    40.4 mL in 1 POUCH; Type 0: Not a Combination Product
    5NDC:0498-0143-333000 in 1 BOX09/18/2018
    50.4 mL in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other09/18/2018
    ALCOHOL PREP PAD 
    isopropyl alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0498-0142
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0498-0142-3410 in 1 BOX01/01/2017
    10.4 mL in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/01/2017
    Labeler - Honeywell Safety Products USA, Inc (118768815)
    Registrant - Honeywell Safety Products USA, Inc (118768815)
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