Label: GOLD BOND ORIGINAL STRENGTH- levomenthol powder
GOLD BOND EXTRA STRENGTH- levomenthol powder

  • NDC Code(s): 41167-0104-0, 41167-0104-1, 41167-0104-3, 41167-0104-6, view more
    41167-0404-0, 41167-0404-1
  • Packager: Chattem, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated January 15, 2016

If you are a consumer or patient please visit this version.

  • SPL UNCLASSIFIED SECTION

    Gold Bond Medicated Original Strength Body Powder

    Drug Facts

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  • Active ingredient

    Menthol 0.15%

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  • Purpose

    Anti-Itch

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  • Uses

    temporarily relieves the pain and itch associated with:

    • minor cuts
    • sunburn
    • insect bites
    • scrapes
    • minor burns
    • minor skin irritations
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  • 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.

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  • 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
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  • Inactive ingredients

    talc, zinc oxide, acacia senegal gum, eucalyptol, methyl salicylate, salicylic acid, thymol, zinc stearate (309-004)



    Gold Bond Medicated Extra Strength Body Powder

    Drug Facts

    Close
  • Active ingredient

    Menthol 0.8%

    Close
  • Purpose

    Anti-Itch

    Close
  • Uses

    temporarily relieves the pain and itch associated with:

    • minor cuts
    • sunburn
    • insect bites
    • scrapes
    • minor burns
    • minor skin irritations
    Close
  • 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.

    Close
  • 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
    Close
  • Inactive ingredients

    talc, zinc oxide, acacia senegal gum, eucalyptol, methyl salicylate, salicylic acid, thymol, zinc stearate (309-006)

    Close
  • PRINCIPAL DISPLAY PANEL

    Gold Bond
    Medicated Healing Since 1908

    Original Strength

    BODY POWDER
    Triple Action Relief
    Cooling ● Absorbing ● Itch Relieving

    Menthol 0.15%
    Net wt 4 oz (113 g)

    Gold Bond
Medicated Healing Since 1908
Original Strength
BODY POWDER
Triple Action Relief
Cooling ● Absorbing ● Itch Relieving
Menthol 0.15%
Net wt 4 oz (113 g)

    Close
  • PRINCIPAL DISPLAY PANEL

    Gold Bond
    Healing Medicated Since 1908
    Extra Strength

    BODY POWDER

    Triple Action Relief
    Cooling ● Absorbing ● Itch Relieving

    Menthol 0.8%
    Net wt 4 oz (113 g)

    Gold Bond
Healing Medicated Since 1908
Extra Strength
BODY POWDER
Triple Action Relief
Cooling ● Absorbing ● Itch Relieving
Menthol 0.8%
Net wt 4 oz (113 g)

    Close
  • INGREDIENTS AND APPEARANCE
    GOLD BOND  ORIGINAL STRENGTH
    menthol powder
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:41167-0104
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    LEVOMENTHOL (UNII: BZ1R15MTK7) (LEVOMENTHOL - UNII:BZ1R15MTK7) LEVOMENTHOL 0.0015 g  in 1 g
    Inactive Ingredients
    Ingredient Name Strength
    TALC (UNII: 7SEV7J4R1U)  
    ZINC OXIDE (UNII: SOI2LOH54Z)  
    ACACIA (UNII: 5C5403N26O)  
    EUCALYPTOL (UNII: RV6J6604TK)  
    METHYL SALICYLATE (UNII: LAV5U5022Y)  
    SALICYLIC ACID (UNII: O414PZ4LPZ)  
    THYMOL (UNII: 3J50XA376E)  
    ZINC STEARATE (UNII: H92E6QA4FV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:41167-0104-0 113 g in 1 BOTTLE; Type 0: Not a Combination Product
    2 NDC:41167-0104-1 28 g in 1 BOTTLE; Type 0: Not a Combination Product
    3 NDC:41167-0104-3 283 g in 1 BOTTLE; Type 0: Not a Combination Product
    4 NDC:41167-0104-6 679 g in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH NOT FINAL part348 04/29/1996
    GOLD BOND  EXTRA STRENGTH
    menthol powder
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:41167-0404
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    LEVOMENTHOL (UNII: BZ1R15MTK7) (LEVOMENTHOL - UNII:BZ1R15MTK7) LEVOMENTHOL 0.008 g  in 1 g
    Inactive Ingredients
    Ingredient Name Strength
    TALC (UNII: 7SEV7J4R1U)  
    ZINC OXIDE (UNII: SOI2LOH54Z)  
    ACACIA (UNII: 5C5403N26O)  
    EUCALYPTOL (UNII: RV6J6604TK)  
    METHYL SALICYLATE (UNII: LAV5U5022Y)  
    SALICYLIC ACID (UNII: O414PZ4LPZ)  
    THYMOL (UNII: 3J50XA376E)  
    ZINC STEARATE (UNII: H92E6QA4FV)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:41167-0404-0 113 g in 1 BOTTLE; Type 0: Not a Combination Product
    2 NDC:41167-0404-1 283 g in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC MONOGRAPH NOT FINAL part348 04/29/1996
    Labeler - Chattem, Inc. (003336013)
    Close