Label: MCKESSON ALCOHOL PREP PAD- isopropyl alcohol swab

  • NDC Code(s): 68599-5804-1, 68599-5804-2, 68599-5804-3, 68599-5804-4, view more
    68599-5804-5, 68599-5804-6
  • Packager: McKesson Medical-Surgical
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 17, 2023

If you are a consumer or patient please visit this version.

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Isopropyl Alcohol 70% v/v

  • Purpose

    First Aid Antiseptic

  • Use

    For preparation of the skin prior to an injection

  • Warnings

    • For external use only
    • Flammable, keep away from fire or flame
  • DO NOT USE

    • Do not use with electrocautery procedures
    • Do not use in the eyes
    • Do not apply to irritated skin

    • Stop use if pain, irritation, redness, or swelling occurs, discontinue use and consult a physician.

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

    • Open packet
    • Remove pad
    • Apply topically as needed to cleanse intended area. Discard after single use.
  • Other information

    • Store at room temperature 59-86°F (15-30°C)
    • Contents sterile in unopened, undamaged package
  • Inactive ingredients

    purified water

  • Principal Display Panel – Box Label

    NDC 68599-5804-2

    MCKESSON

    Alcohol Prep Pads

    STERILE | SATURATED WITH 70% v/v ISOPROPYL ALCOHOL

    1.2" x 2.6"
    (3 cm x 6.5 cm)

    200
    PER BOX

    DO NOT REUSE

    MFR# 58-204

    Principal Display Panel – Box Label
  • Principal Display Panel – Packet Label

    NDC 68599-5804-1

    MCKESSON

    Alcohol Prep Pad

    STERILE | SATURATED WITH
    70% v/v ISOPROPYL ALCOHOL

    1.2" x 2.6"
    (3 cm x 6.5 cm)

    DO NOT
    REUSE

    MFR# 58-204

    Principal Display Panel – Packet Label
  • INGREDIENTS AND APPEARANCE
    MCKESSON ALCOHOL PREP PAD 
    isopropyl alcohol swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68599-5804
    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:68599-5804-320 in 1 CASE04/09/2010
    1NDC:68599-5804-2200 in 1 BOX
    1NDC:68599-5804-11 mL in 1 PACKET; Type 0: Not a Combination Product
    2NDC:68599-5804-610 in 1 CASE04/09/2010
    2NDC:68599-5804-5100 in 1 BOX
    2NDC:68599-5804-41 mL in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00304/09/2010
    Labeler - McKesson Medical-Surgical (023904428)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shandong Haiyan Medical421283439manufacture(68599-5804)
    Establishment
    NameAddressID/FEIBusiness Operations
    Jiangsu Province Jianerkang Medical Dressing Co., Ltd530968767manufacture(68599-5804)
    Establishment
    NameAddressID/FEIBusiness Operations
    Phoenix Innovative Healthcare650743854manufacture(68599-5804)