Label: MEDPRIDE PREPPADS- povidone iodine solution

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 14, 2023

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  • Active Ingredient

    Povidone Iodine 10% v/v

    (equivalent to 1% titratable iodine)

  • Purpose

    Antiseptic

  • Uses

    ■ health care antiseptic for preparation of the skin prior to surgery

    ■ first aid antiseptic to help prevent the risk of skin infection in minor cuts, scrapes and burns

  • Warnings

    For external use only

  • Do not use

    ■ in the eyes

    ■ on individuals who are allergic or sensitive to iodine

    ■ over large areas of the body

    ■ as first aid antiseptic for more than 1 week unless directed by doctor

  • Ask a doctor before use if you have

    ■ deep or puncture wounds

    ■ animal bites

    ■ serious burns

  • Stop use and ask a doctor if

    ■ condition worsens or persists fro more than 72 hours ■ irritation and rednesss develops

  • Keep out of reach of children

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

  • Directions

    ■ for preparation of the skin prior to surgery, clean the affected area, remove the pad, apply to the operative site prior to surgery

    ■ for use as a first aid antiseptic, clean the affected area, apply a small amount of this product on the area 1-3 times daily ■ may be covered with a sterile bandage ■ if bandaged, let dry first

  • Other Information

    ■ store at room temperature:15-30C (59-86F)

  • Inactive Ingredients

    Citric Acid Monohydrate, Sodium Phosphate Dibasic, Water

  • Package Label

    Principal Display

  • INGREDIENTS AND APPEARANCE
    MEDPRIDE  PREPPADS
    povidone iodine solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52410-4115
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE0.1 g
    Inactive Ingredients
    Ingredient NameStrength
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52410-4115-3100 in 1 BOX; Type 0: Not a Combination Product10/20/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00310/20/2018
    Labeler - Shield Line LLC (078518916)
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