Label: POVIDONE-IODINE 10% SOLUTION- povidone iodine 10% liquid liquid

  • NDC Code(s): 82429-202-16
  • Packager: Gabar Health Sciences Corp.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 21, 2023

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  • ACTIVE INGREDIENT

    ​POVIDONE IODINE 10%

  • Warnings

    For external use only

  • ​Do Not Use

    • if allergic to iodine
    • in the eyes
  • ​Stop use and ask a doctor if

    • irritation and redness develop
    • condition persists for more than 72 hours
  • KEEP OUT OF REACH OF CHILDREN

    ​Keep out of reach of children. ​ If swallowed, get medical help, or contact a Posion Control Center (1-800-222-1222) right away.

  • ​Inactive Ingredients

    Povidone-iodine 10%

  • ​Purpose

    Healthcare Antiseptic

  • ​Use

    For preparation of the skin prior to surgery. Helps reduce bacteria that potentially can cause skin infection

  • ​Use

    For preparation of the skin prior to surgery. Helps reduce bacteria that potentially can cause skin infection.

  • ​Directions

    Clean the area. Apply product to the operative site prior to surgery.

  • Other

    Store at controlled room temperature 15º-30ºC (59º-86ºF).

  • ​Questions?

    1-470-737-9424

  • Principal Display Panel

    ​NDC 82429-202-16

    Gabar Health Sciences

    Povidone-Iodine

    10% Solution

    Topical Antiseptic

    ​1 Gallon (3.78 L)

    Povidone-Iodine Label

  • INGREDIENTS AND APPEARANCE
    POVIDONE-IODINE 10% SOLUTION 
    povidone iodine 10% liquid liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82429-202
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    POVIDONE-IODINE (UNII: 85H0HZU99M) (IODINE - UNII:9679TC07X4) IODINE10 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    SODIUM PHOSPHATE DIBASIC DIHYDRATE (UNII: 94255I6E2T)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82429-202-163780 mL in 1 PACKAGE; Type 0: Not a Combination Product10/10/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00310/10/2022
    Labeler - Gabar Health Sciences Corp. (118401847)
    Registrant - Gabar Health Sciences Corp. (118401847)
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