Label: BD E-Z SCRUB- povidone-iodine solution

  • NDC Code(s): 17271-503-01
  • Packager: Becton Dickinson and Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 30, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Povidone-Iodine 6.5% w/w (minimum available Iodine 0.5%)

  • Purpose

    Antiseptic

  • Uses

    • surgical hand scrub: significantly reduces the number of microorganisms on the hands and forearms prior to surgery or patient care
    • healthcare personnel handwash: helps reduce bacteria that potentially can cause disease
  • Warnings

    For external use only

    Do not use if redness or irritation occurs

    When using this product avoid contact with eyes

    Stop use and ask a doctor if severe adverse reactions occur

    Keep out of reach of children. If swallowed or gets in eyes, get medical help or contact a Poison

    Control Center right away.

  • Directions

    Surgical Hand Scrub

    • Wet hands and forearms with warm water
    • Use nail cleaner and then apply solution from the sponge side to work up a lather
    • Scrub thoroughly for 3 minutes: difficult areas (interdigital space and fingers) with brush side, hands and forarms with sponge side
    • Rinse thoroughly with warm water
    • Repeat scrub for 3 minutes, sponge side only
    • Rinse hands and arms thoroughly
    • Dry thoroughly

    Health Care Personnel Handwash

    • Dispense about 5 ml of foam solution into cupped hands
    • Wash in a vigorous manner covering all surfaces for 30 seconds
    • Rinse thoroughly with running water (30 seconds)
  • Other information

    avoid excessive heat above 104°F (40°C)

  • Inactive ingredients

    ammonium nonoxynol sulfate, disodium phosphate, hydrogen peroxide, octoxynol, phosphoric acid, sodium hydroxide, water

  • Questions?

    1-800-453-4538 Monday to Friday, 8 a.m. to 5 p.m. MST

  • PRINCIPAL DISPLAY PANEL

    Principal Display Panel – Bottle Label

    BD E-Z Scrub™
    0.5% Povidone
    Iodine Antiseptic
    Solution

    REF 372405 • NDC 17271-503-01

    Foreign Patents and Patents Pending.
    U.S. Patents 6,053,369 - 6,308,866

    32 FL. OZ (946 ml)

    Povidone-Iodine

    Principal Display Panel – Bottle Label
  • INGREDIENTS AND APPEARANCE
    BD E-Z SCRUB 
    povidone-iodine solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:17271-503
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE50 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    AMMONIUM NONOXYNOL-4 SULFATE (UNII: 9HIA70O4J0)  
    SODIUM PHOSPHATE, DIBASIC, DIHYDRATE (UNII: 94255I6E2T)  
    HYDROGEN PEROXIDE (UNII: BBX060AN9V)  
    OCTOXYNOL 9 (UNII: 7JPC6Y25QS)  
    PHOSPHORIC ACID (UNII: E4GA8884NN)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:17271-503-016 in 1 BOX04/01/200001/31/2025
    1946 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)04/01/200001/31/2025
    Labeler - Becton Dickinson and Company (124987988)
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