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PDI Alcohol Prep Pad Sterile (Professional Disposables International, Inc.)

Available Formats

Dosage Form Package Information Links
CLOTH 100 PACKET in 1 BOX (10819-3914-2) > 1.6 mL in 1 PACKET Label Information
CLOTH 200 PACKET in 1 BOX (10819-3914-1) > .62 mL in 1 PACKET Label Information

Complete PDI Alcohol Prep Pad Sterile Information

  • Active ingredient

    Isopropyl Alcohol 70% v/v

  • Purpose


  • Use

    For preparation of skin prior to an injection

  • Warnings

    For external use only.

    Flammable, keep away from fire or flame.

  • Do not

    • use with electrocautery preocedures
    • use in the eyes
    • apply on irritated skin

  • Stop use if

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

  • Keep out of reach of children

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

  • Directions

    Wet topically and discard after single use

  • Other information

    Store at room temperature (15-30ºC) (59-86ºF)

  • Inactive ingredient

    Purified Water

  • Principal display panel

    Alcohol Prep Pad


    Medium or Large


    Sterile solution

    Applicator is sterile if package is intact

    For Hospital and Home Use Settings

    Dispose of used wipes in trash receptacle. Do not flush.

    Professional Disposables International, Inc.
    Orangeburg, NY 10962-1376
    USA - 1800-999-6423

    Packet Medium:

    Packet Medium
    Box Medium:

    Box Medium

    Packet Large:

    Packet large
    Box Large:

    box large

    alcohol cloth
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:10819-3914
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL 0.7 mL  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R) 0.3 mL  in 1 mL
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:10819-3914-2 100 in 1 BOX 01/01/1972
    1 1.6 mL in 1 PACKET; Type 0: Not a Combination Product
    2 NDC:10819-3914-1 200 in 1 BOX 01/01/1972
    2 0.62 mL in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part333A 01/01/1972
    Labeler - Professional Disposables International Inc (800777117)
    Registrant - Professional Disposables International inc (800777117)
    Name Address ID/FEI Business Operations
    Professional Disposables International Inc 800777117 manufacture(10819-3914)