Label: GOLD BOND MEDICATED MAXIMUM STRENGTH FOOT- menthol powder

  • NDC Code(s): 41167-0171-2, 41167-0171-6
  • Packager: Chattem, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 30, 2023

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  • SPL UNCLASSIFIED SECTION

    Gold Bond Medicated

    Foot Powder

    Drug Facts

  • Active ingredient

  • Purpose

    Menthol 1%......................................................................................................................................................Anti-itch

  • Uses

    temporarily relieves the pain and itch associated with:

    ■ minor skin irritations on the foot  

  • Warnings

    For external use only

    When using this product

    ■ avoid contact with eyes  

    Stop use and ask a doctor if

    ■ condition worsens

    ■ symptoms persist for more than 7 days or clear up and occur again within a few days

    ■ redness, irritation, swelling or pain persists or increases

    Keep out of reach of children.

    If swallowed, get medical help or contact a Poison Control Center immediately.

  • Directions

    ■ adults and children 2 years and older: apply freely up to 3 or 4 times daily  

    ■ children under 2 years: ask a doctor

    ■ thoroughly wash and dry feet, sprinkle powder liberally over feet, between toes and on bottoms of feet. Sprinkle inside shoes for maximum freshness.

  • Inactive ingredients

    zea mays (corn) starch, sodium bicarbonate, acacia senegal gum, silica, tricalcium phosphate, eucalyptus globulus leaf oil, mentha piperita (peppermint) oil, benzethonium chloride

  • PRINCIPAL DISPLAY PANEL

    TALC-FREE
    GOLD BOND
    MAXIMUM STRENGTH
    FOOT POWDER
    Net Wt 10 oz (283 g)

    PRINCIPAL DISPLAY PANEL TALC-FREE GOLD BOND MAXIMUM STRENGTH FOOT POWDER Net Wt 10 oz (283 g)  PRINCIPAL DISPLAY PANEL TALC-FREE GOLD BOND MAXIMUM STRENGTH FOOT POWDER Net Wt 10 oz (283 g)

  • INGREDIENTS AND APPEARANCE
    GOLD BOND MEDICATED MAXIMUM STRENGTH FOOT 
    menthol powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41167-0171
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL1 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    STARCH, CORN (UNII: O8232NY3SJ)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    ACACIA (UNII: 5C5403N26O)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    TRICALCIUM PHOSPHATE (UNII: K4C08XP666)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    BENZETHONIUM CHLORIDE (UNII: PH41D05744)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41167-0171-2283 g in 1 BOTTLE; Type 0: Not a Combination Product03/01/2021
    2NDC:41167-0171-6113 g in 1 BOTTLE; Type 0: Not a Combination Product03/01/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01703/01/2021
    Labeler - Chattem, Inc. (003336013)
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