Label: IODINE liquid

  • NDC Code(s): 41163-088-10
  • Packager: United Natural Foods, Inc. dba UNFI
  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated May 10, 2023

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  • Active Ingredient

    Iodine tincture U.S.P. 100% (2% iodine)

  • Purpose

    First aid antiseptic

  • Use

    First aid to help prevent skin infection in

    • minor cuts
    • scrapes
    • burns
  • Warnings

    For external use only

  • Ask a doctor before use if you have

    deep or puncture wounds, animal bites or serious burns

  • When using this product

    • do not use in eyes or apply over large areas of the body
    • do not use longer than 1 week unless directed by a doctor
  • 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 right away.

  • Directions

    • clean the affected area
    • apply a small amount on the area 1 to 3 times daily
    • may be covered with a sterile bandage
    • if bandaged, let dry first
  • Inactive ingredients

    Not Listed: alcohol (47% v/v), purified water, sodium iodide

  • Other information

    Product will stain skin and clothing

  • SPL UNCLASSIFIED SECTION

    Distributed by UNFI, Eden Prairie, MN 55344 USA

    Contact us at 1-877-932-7948 or www.supervalu-ourownbrands.com

  • Principal display panel

    NDC 41163-088-10

    EQUALINE

    iodine tincture USP

    first aid antiseptic

    for external use only

    CAUTION POISON

    1 OZ (30 mL)

    image description

  • INGREDIENTS AND APPEARANCE
    IODINE 
    iodine liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41163-088
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4) IODINE20 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    water (UNII: 059QF0KO0R)  
    SODIUM IODIDE (UNII: F5WR8N145C)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41163-088-1030 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/04/2005
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A02/04/2005
    Labeler - United Natural Foods, Inc. dba UNFI (943556183)
    Registrant - Vi-Jon, LLC (790752542)
    Establishment
    NameAddressID/FEIBusiness Operations
    Pharma Nobis118564114manufacture(41163-088)
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