Label: MEDICHOICE POVIDONE-IODINE- povidone-iodine ointment

  • NDC Code(s): 39892-0820-1
  • Packager: Owens & Minor Distribution, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 9, 2023

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  • Drug Facts

  • Active ingredient

    Povidone-iodine USP 10%

    Purpose

    Antiseptic

  • Use

    Antiseptic skin preparation

  • Warnings

    For external use only.

    Do not use

    • if allergic to iodine
    • in the eyes

    Keep out of reach of children.

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

    Ask a doctor before use

    if injuries are deep wounds, puncture wounds, or serious burns.

    Stop use and ask a doctor

    if infection occurs or if redness, irritation, swelling or pain persists or increases.

  • Directions

    Apply locally as needed.

  • Other information

    • 1% titratable iodine
    • FOR HOSPITAL OR PROFESSIONAL USE ONLY.
  • Inactive ingredients

    Carbomer, Glycerin, Purified Water

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    MEDICHOICE POVIDONE-IODINE 
    povidone-iodine ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:39892-0820
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE100 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:39892-0820-11 g in 1 PACKET; Type 0: Not a Combination Product03/04/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)03/04/2019
    Labeler - Owens & Minor Distribution, Inc. (847412269)
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