Label: POVIDONE-IODINE SCRUB STERILE- povidone-iodine swab

  • NDC Code(s): 63517-252-21
  • Packager: Cardinal Health 200, Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 10, 2023

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  • Drug Facts

  • Active ingredient

    Povidone-Iodine 7.5%

    Purpose

    Antiseptic

  • Use

    • For preparation prior to surgery • Helps to reduce bacteria that can potentially cause skin infection

  • Warnings

    ​For external use only.

    Do not apply to persons allergic to iodine

    Do not use

    • in the eyes

    Ask a doctor before use if injuries are

    • deep wounds • puncture wounds • serious burns

    Stop use and ask a doctor if

    • irritation and redness develop • condition persists for more than 72 hours • infection occurs

    Avoid pooling beneath the patient.

    Prolonged exposure to wet solution may cause skin irritation.

    Keep out of reach of children.

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

  • Directions

    Clean the area. Apply product to the operative site prior to surgery using sponge sticks to prep desired area.

  • Other information

    • saturating solution contains 0.75% titratable iodine • latex free • for hospital or professional use only

  • Inactive ingredients

    Citric Acid, Alkyl Glucoside, Nonoxynol-10, Glycerin, Sodium Hydroxide, Potassium Iodide, Purified Water

  • Product Label

    BoxLabel

  • INGREDIENTS AND APPEARANCE
    POVIDONE-IODINE SCRUB STERILE 
    povidone-iodine swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63517-252
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE75 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    NONOXYNOL-10 (UNII: K7O76887AP)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    POTASSIUM IODIDE (UNII: 1C4QK22F9J)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63517-252-2150 in 1 BOX04/29/2015
    11 in 1 POUCH
    12 g in 1 POUCH; Type 4: Device Coated/Impregnated/Otherwise Combined with Drug
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)04/29/2015
    Labeler - Cardinal Health 200, Inc (961027315)
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