Label: MOAKANG POVIDONE-IODINE SCRUB WINGED SPONGES- povidone-iodine solution

  • NDC Code(s): 59050-267-00
  • Packager: Changzhou Maokang Medical Products Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 9, 2023

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  • Drug Facts

  • Active ingredient

    Povidone Iodine 10% w/w

    Purpose

    Antiseptic

  • Use

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

    • Do not apply to persons allergic to iodine

    Ask a doctor before use if injuries are

    • deep wounds
    • puncture wounds
    • serious burns

    Stop use and ask a doctor if

    • redness, irritation, swelling or pain persists or increases 
    • infection occurs
    • Prolonged exposure to wet solution may cause skin irritation.
    • Store at room temperature.

    Avoid pooling beneath the patient.

    Avoid excessive heat.

    Keep out of reach of children.

    • In case of accidental ingestion, seek professional assistance or consult a poison control center immediately.
  • Directions

    • use sponges to prep desired area
  • Other information

    • 1% titratable iodine
    • for hospital or professional use only

    For external use only

  • Inactive ingredients

    Nonoxynol-10, alkyl glucoside, potassium iodide, sodium hydroxide, glycerin, anhydrous citric acid, Sodium dodecyl sulfate, purified water

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    MOAKANG POVIDONE-IODINE SCRUB WINGED SPONGES 
    povidone-iodine solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59050-267
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE100 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    NONOXYNOL-10 (UNII: K7O76887AP)  
    POTASSIUM IODIDE (UNII: 1C4QK22F9J)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59050-267-00122.17 mL in 1 POUCH; Type 0: Not a Combination Product07/20/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)07/20/2023
    Labeler - Changzhou Maokang Medical Products Co., Ltd (421317073)
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