Label: MG217 FIRST AID DRAWING SALVE- ichthammol ointment

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated January 13, 2022

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  • PURPOSE

    For drawing or removing splinters, slivers, or similar items

  • Drug Facts

    Active ingredientsPurpose
    Ichthammol USP 10%Drawing Salve

  • Uses

    For drawing or removing splinters, slivers, or similar ijems

  • Warnings

    For external use only

    Do not use in eyes.

    Ask a doctor before use if you have deep puncture wounds or serious burns.

    Stop use and ask a doctor if redness, irritation, swelling or pain persists.

    Keep out of reach of chlldren. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    Cleanse affected area. Apply on gauze bandage once or twice a day. Repeat as necessary. Do not rub or massaoe affected area.

  • Other information

    Store at room temperature.

  • Inactive ingredients

    Bis-diglyceryl polyacyladipate-2, Petrolatum

  • Questions or comments?

    1-800-635-3696

  • Package Label

    Tube Label

  • Package Label

    Carton

  • INGREDIENTS AND APPEARANCE
    MG217 FIRST AID DRAWING SALVE 
    ichthammol ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68093-7218
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ICHTHAMMOL (UNII: NQ14646378) (ICHTHAMMOL - UNII:NQ14646378) ICHTHAMMOL100 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    BIS-DIGLYCERYL POLYACYLADIPATE-2 (UNII: 6L246LAM9T)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    Product Characteristics
    Colorbrown (To dark brown paste) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68093-7218-11 in 1 CARTON07/01/2020
    128.3 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other07/01/2020
    Labeler - Wisconsin Pharmacal Company (800873986)
    Registrant - Wisconsin Pharmacal Company (800873986)
    Establishment
    NameAddressID/FEIBusiness Operations
    Wisconsin Pharmacal Company800873986manufacture(68093-7218) , pack(68093-7218) , label(68093-7218)