Label: GOLD BOND MEDICATED ORIGINAL STRENGTH BODY- menthol powder

  • NDC Code(s): 41167-0110-6, 41167-0110-9
  • 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

    Original Strength Body Powder

    Drug Facts

  • Active ingredient

  • Purpose

    Menthol 0.15%................................................................................................................................................       Anti-itch

  • Uses

    temporarily relieves the pain and itch associated with:

    ■ minor cuts  ■ sunburn  ■ insect bites  ■ scrapes ■ minor burns ■ minor skin irritations   

  • 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

    ■ for best results dry skin thoroughly before applying

  • Inactive ingredients

    zea mays (corn) starch, zinc oxide, acacia senegal gum, silica, tricalcium phosphate, eucalyptol, methyl salicylate, salicylic acid, zinc stearate, thymol

  • PRINCIPAL DISPLAY PANEL

    GOLD BOND
    ORIGINAL STRENGTH
    BODY POWDER
    Net Wt 10 oz (283 g)

    PRINCIPAL DISPLAY PANEL GOLD BOND ORIGINAL STRENGTH BODY POWDER Net Wt 10 oz (283 g)  PRINCIPAL DISPLAY PANEL GOLD BOND ORIGINAL STRENGTH BODY POWDER Net Wt 10 oz (283 g)

  • INGREDIENTS AND APPEARANCE
    GOLD BOND MEDICATED ORIGINAL STRENGTH BODY 
    menthol powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41167-0110
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL0.15 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    STARCH, CORN (UNII: O8232NY3SJ)  
    ZINC OXIDE (UNII: SOI2LOH54Z)  
    ACACIA (UNII: 5C5403N26O)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    TRICALCIUM PHOSPHATE (UNII: K4C08XP666)  
    EUCALYPTOL (UNII: RV6J6604TK)  
    METHYL SALICYLATE (UNII: LAV5U5022Y)  
    SALICYLIC ACID (UNII: O414PZ4LPZ)  
    ZINC STEARATE (UNII: H92E6QA4FV)  
    THYMOL (UNII: 3J50XA376E)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41167-0110-9283 g in 1 BOTTLE; Type 0: Not a Combination Product03/01/2021
    2NDC:41167-0110-6113 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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