Label: IODINE liquid

  • NDC Code(s): 11344-880-10
  • Packager: Consumer Product Partners, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 4, 2024

If you are a consumer or patient please visit this version.

View All Sections
  • 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 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
  • Other information

    product will stain skin and clothing

  • SPL UNCLASSIFIED SECTION

    Vi-Jon One Swan Drive, Smyrna, TN 37167

  • Inactive ingredients

    alcohol (47% v/v), purified water, sodium iodide

  • Principal display panel

    FOR EXTERNAL USE ONLY

    Swan ®

    Iodine Tincture U.S.P.

    • First Aid Antiseptic

    CAUTION POISON

    1 FL OZ (30 mL)

    image description

  • INGREDIENTS AND APPEARANCE
    IODINE 
    iodine liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11344-880
    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:11344-880-1030 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product08/07/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00308/07/2017
    Labeler - Consumer Product Partners, LLC (119091520)
    Registrant - Consumer Product Partners, LLC (119091520)
    Establishment
    NameAddressID/FEIBusiness Operations
    Consumer Product Partners, LLC119091514manufacture(11344-880)
    Establishment
    NameAddressID/FEIBusiness Operations
    Pharma Nobis, LLC118564114manufacture(11344-880)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!