Label: GOLD BOND ANTI ITCH- menthol and pramoxine hydrochloride cream

  • NDC Code(s): 41167-0501-0, 41167-0501-1, 41167-0501-2
  • Packager: Chattem, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 3, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredients

    Menthol 1%

    Pramoxine hydrochloride 1%

  • Purpose

    Anti-itch, Pain relief

  • Uses

    for temporary relief of pain and itching associated with:

    • minor skin irritations
    • minor cuts
    • minor burns
    • minor sunburns
    • rashes due to poison ivy, poison oak or poison sumac
    • scrapes
    • insect bites
  • Warnings

    For external use only

    Do not use on

    • deep or puncture wounds
    • animals 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 last more than 7 days or clear up and occur again within a few days
    • if 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 to affected area up to 3 or 4 times daily

    children under 2 years: consult a doctor

  • Inactive ingredients

    water, petrolatum, propylene glycol, stearyl alcohol, aloe barbadensis leaf juice, triethanolamine, sodium acrylates copolymer, steareth-21, mineral oil, steareth-2, tocopheryl acetate, thymol, eucalyptol, methyl salicylate, PPG-1 trideceth-6,diazolidinyl urea, disodium EDTA, , iodopropynyl butylcarbamate 

  • PRINCIPAL DISPLAY PANEL

    RAPID RELIEF GOLD BOND® 
    Net wt 1 oz (28 g)
    ANTI-ITCH CREAM

    RAPID RELIEF GOLD BOND® Net wt 1 oz (28 g) ANTI-ITCH CREAM

  • INGREDIENTS AND APPEARANCE
    GOLD BOND ANTI ITCH 
    menthol and pramoxine hydrochloride cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41167-0501
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL0.01 g  in 1 g
    PRAMOXINE HYDROCHLORIDE (UNII: 88AYB867L5) (PRAMOXINE - UNII:068X84E056) PRAMOXINE HYDROCHLORIDE0.01 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    STEARETH-21 (UNII: 53J3F32P58)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    STEARETH-2 (UNII: V56DFE46J5)  
    .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
    THYMOL (UNII: 3J50XA376E)  
    EUCALYPTOL (UNII: RV6J6604TK)  
    METHYL SALICYLATE (UNII: LAV5U5022Y)  
    PPG-1 TRIDECETH-6 (UNII: 1K7417JX6Q)  
    DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41167-0501-01 in 1 CARTON04/01/1996
    128 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:41167-0501-11 in 1 CARTON04/01/199602/27/2019
    235 g in 1 TUBE; Type 0: Not a Combination Product
    3NDC:41167-0501-21 in 1 CARTON04/01/199602/28/2019
    356 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01704/01/1996
    Labeler - Chattem, Inc. (003336013)
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