Label: GOLD BOND EXTRA STRENGTH- menthol lotion

  • NDC Code(s): 41167-0641-2, 41167-0641-4
  • 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

    Drug Facts – Extra Strength Gold Bond Body Lotion

  • Active ingredients

    Menthol 0.5%

  • Purpose

    Anti-itch

  • Uses

    temporarily relieves the pain and itching associated with:

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

    For external use only

    Do not use on

    • deep or puncture wounds
    • animal bites
    • serious burns
    • large areas of the body

    When using this product

    • do not get into eyes or nose
    • not for prolonged use

    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 right away.

  • Directions

    adults and children 2 years and older: apply to affected area up to 3 or 4 times daily

    children under 2 years: ask a doctor

  • Inactive ingredients

    water, dimethicone, glycerin, petrolatum, aloe barbadensis leaf juice, cetyl alcohol, stearyl alcohol, propylene glycol, stearamidopropyl PG-dimonium chloride phosphate, distearyldimonium chloride, cetearyl alcohol, polysorbate 60, steareth-21, steareth-2, tocopheryl acetate, EDTA, imidazolidinyl urea, methylparaben, potassium hydroxide, fragrance

  • PRINCIPAL DISPLAY PANEL

    GOLD BOND® 
    EXTRA STRENGTH
    BODY LOTION
    Triple Action Relief
    For Extra Dry & Itchy Skin
    Net wt 14 oz (396 g)

    GOLD BOND® EXTRA STRENGTH BODY LOTION Triple Action Relief For Extra Dry & Itchy Skin Net wt 14 oz (396 g)

  • INGREDIENTS AND APPEARANCE
    GOLD BOND EXTRA STRENGTH 
    menthol lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41167-0641
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL0.005 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    STEARAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE (UNII: W6000VEI5Y)  
    DISTEARYLDIMONIUM CHLORIDE (UNII: OM9573ZX3X)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    STEARETH-21 (UNII: 53J3F32P58)  
    STEARETH-2 (UNII: V56DFE46J5)  
    .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    IMIDUREA (UNII: M629807ATL)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41167-0641-2396 g in 1 BOTTLE; Type 0: Not a Combination Product03/11/2016
    2NDC:41167-0641-4476 g in 1 BOTTLE; Type 0: Not a Combination Product03/11/201609/30/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01703/11/2016
    Labeler - Chattem, Inc. (003336013)
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