Label: ARTHRITIS WONDER- menthol cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by 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 March 27, 2020

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  • Active ingredient

    Menthol 1.25%

  • Purpose

    External analgesic

  • Uses

    For the temporary relief of minor aches and pains of muscles and joints associated with ● arthritis ● simple backache ● strains ● bruises ● sprains

  • Warnings

    For external use only.

    Flammable: Keep away from fire or flame.

    When using this product

    • avoid contact with the eyes • do not bandage tightly

    Do not use

    ● on wounds or damaged skin with a heating pad

    Stop use and ask a doctor if

    • condition worsens • symptoms persist for more than 7 days • symptoms clear up and occur again within a few days

    Keep out of the reach of children

    If swallowed, get medical help or contact a Poison Control Center right away

  • Directions

    • Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily • Children under 2 years of age: consult a doctor

  • Inactive ingredients:

    Alcohol, Caprylic/Capric Triglyceride, Caprylyl Glycol, Cetearyl Alcohol, Cetyl Alcohol, Dimethicone, Ethoxydiglycol, Ethylhexylglycerin, Glyceryl Oleate, Glyceryl Stearate, Hexylene Glycol, Lecithin, Mentha Piperita (Peppermint) Oil, Phenoxyethanol, Potassium Olivoyl Hydrolyzed Oat Protein, Propanediol, Pullulan, Sclerotium Gum, Sodium Phytate, Water, Wogonin, Xanthan Gum.

  • DOSAGE & ADMINISTRATION

  • Principal Display Panel

    Principal Display Panel

  • INGREDIENTS AND APPEARANCE
    ARTHRITIS WONDER 
    menthol cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71893-101
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL1.4125 g  in 113 g
    Inactive Ingredients
    Ingredient NameStrength
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)  
    LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    GLYCERYL OLEATE (UNII: 4PC054V79P)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    PULLULAN (UNII: 8ZQ0AYU1TT)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    WATER (UNII: 059QF0KO0R)  
    WOGONIN (UNII: POK93PO28W)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    ALCOHOL (UNII: 3K9958V90M)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    CLAVICEPS PURPUREA SCLEROTIUM (UNII: 01G9XEA93N)  
    HEXASODIUM PHYTATE (UNII: ZBX50UG81V)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71893-101-2085 g in 1 APPLICATOR; Type 0: Not a Combination Product04/26/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34804/06/2020
    Labeler - G2 Products LLC (080963729)
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