Label: IODINE PREP PAD ANTISEPTIC- povidone-iodine solution

  • NDC Code(s): 72459-017-01
  • Packager: Yiwu Ori-Power Medtech Co.,Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 26, 2024

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  • DRUG FACTS

  • Active Ingredients

    Povidone Iodine 10% USP.

    Purpose

    First aid to help reduce the risk of infection in minor cuts, scrapes, and burns.

  • Inactive Ingredients

    Citric Acid, Glucoside, Hydroxyethyl Cellulose, Nonoxynol-10, Glycerin, Sodium Hydroxide, Potassium Iodide, Purified Water.

  • Use

    Topical Antimicrobial Agent For Wound Disinfection.

  • Directions

    Tear open packet, use Iodine-saturated pad to cleanse desired skin area. Discard pad appropriately after use.

  • Storage

    Store at room temperature 15°C - 30°C (59°F - 86°F).

  • Warnings

    Avoid contact with eyes. If happens, rinse thoroughly with water. For External Use Only. If pain, irritation, redness, swelling, or infection develops, discontinue use and consult physician.

    Keep Out  Of Reach Of Children

    In case of accidental swallowing, seek medical help and contact poison control immediately.

  • Package Labeling:

    Label3

  • INGREDIENTS AND APPEARANCE
    IODINE PREP PAD ANTISEPTIC 
    povidone-iodine solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72459-017
    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
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    .BETA.-D-GLUCOPYRANOSE (UNII: J4R00M814D)  
    HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)  
    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:72459-017-010.55 g in 1 POUCH; Type 0: Not a Combination Product02/01/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00302/01/2024
    Labeler - Yiwu Ori-Power Medtech Co.,Ltd. (560451976)
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