Label: SALICYLIC IODINE (IODO SALICILICO) FIRST AID ANTISEPTIC- iodine 2% liquid

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

Drug Label Information

Updated October 27, 2023

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  • Active Ingredient

    Iodine 2%

  • Purpose

    First aid antiseptic

  • Uses

    As a first aid to help prevent skin infection in minor cuts, scrapes and 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

  • Ask a Doctor before use if

    If you have deep or puncture wounds, animal bites or serious burns.

  • Keep out of reach of children.

    Keep out of the 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.

  • Inactive Ingredients

    Alcohol, salicylic acid, and water.

  • Questions or Comments

    1-305-256-1464

  • Principal Display Panel

    Iodo SalicylicSalicylic Iodine 2%

  • INGREDIENTS AND APPEARANCE
    SALICYLIC IODINE (IODO SALICILICO)  FIRST AID ANTISEPTIC
    iodine 2% liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73635-1220
    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
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    SALICYLIC ACID (UNII: O414PZ4LPZ)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73635-1220-130 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product03/29/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00303/29/2021
    Labeler - Germa Products, LLC (116626935)
    Registrant - Germa Products, LLC (116626935)
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