Label: ICHTHAMMOL- ichthammol ointment 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 October 31, 2023

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  • Active Ingredient

    Ichthammol USP 10%

  • Purpose

    Drawing Salve

  • Uses

    for drawing or removing splinters, silvers, or similar items.

  • 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 doctor if

    redness, irritation, swelling or pain persists.

    Keep out of reach of children

    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 massage affected area.

  • Other information

    Store at room temperature.

  • Inactive ingredients

    Bis-diglyceryl Polyacyladipate-2, Petrolatum

  • Questions or comments?

    1-800-925-4733

  • Carton

    Package Label

  • INGREDIENTS AND APPEARANCE
    ICHTHAMMOL 
    ichthammol ointment ointment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-2052
    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
    PETROLATUM (UNII: 4T6H12BN9U)  
    BIS-DIGLYCERYL POLYACYLADIPATE-2 (UNII: 6L246LAM9T)  
    Product Characteristics
    Colorbrown (Brownish Black ointment) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0363-2052-2828 g in 1 TUBE; Type 0: Not a Combination Product07/28/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other07/28/2021
    Labeler - Walgreens (008965063)