Label: POVIDONE IODINE PREP PAD- antiseptic swab

  • NDC Code(s): 67777-002-01, 67777-002-02, 67777-002-03, 67777-002-04
  • Packager: Dynarex Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 24, 2024

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  • Active Ingredient

    Povidone-Iodine USP 10% w/v (9.85% w/w)

  • Purpose

    First Aid Antiseptic

  • Use(s)

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

  • Warnings

    For External Use Only

    Do not use

    • In the eyes or over large areas of the body

    • Longer than one week unless directed by a 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 persists or gets worse

    Keep out of reach of children

    If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

  • Directions

    • Tear at notch
    • Remove prep pad
    • Apply a small amount of this product on the area 1 to 3 times daily.
    • May be covered with a sterile bandage
    • If bandaged, let dry first
    • Use only once

  • Other Information

    • Store at room temperature 15º-30ºC (59º-86ºF)
    • Flammable. Keep away from fire or flame
  • Inactive Ingredients

    Anhydrous Citric Acid, Glycerin, Polysorbate 80, Sodium Citrate, Sodium Phosphate Dibasic, Water

  • Label

    Povidone-Iodine Prep Pads

  • Label

    1108 BX MASTERPovidon Iodine Prep Pad

  • Label 1108UB-10

    1108UB-10_BX_MASTER1108UB-10

  • INGREDIENTS AND APPEARANCE
    POVIDONE IODINE PREP PAD 
    antiseptic swab
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67777-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE10 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    Product Characteristics
    Color    Score    
    ShapeRECTANGLESize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67777-002-011000 in 1 CASE12/17/2018
    1NDC:67777-002-02100 in 1 BOX
    10.3 g in 1 PACKET; Type 0: Not a Combination Product
    2NDC:67777-002-031000 in 1 CASE12/17/2018
    2NDC:67777-002-0410 in 1 BOX
    20.3 g in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00312/17/2018
    Labeler - Dynarex Corporation (008124539)
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