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 January 27, 2020

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

  • 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:

    Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf Juice, Butylene Glycol, Caprylic/Capric Triglyceride, Caprylyl Glycol, Ceteareth-20, Cetearyl Alcohol, Dimethicone, Dimethyl Sulfone, Ethoxydiglycol, Ethylhexylglycerin, Glycerin, Glyceryl Stearate, Hexylene Glycol, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Mentha Piperita (Peppermint) Oil, PEG-100 Stearate, Phenoxyethanol, Polysorbate 60, Prunus Amygdalus Dulcis (Sweet Almond) Oil, Sorbitan Isostearate, Squalane, Stearic Acid, Tetrasodium Glutamate Diacetate, Water, Wogonin, Xanthan Gum

  • DOSAGE & ADMINISTRATION

  • Principal Display Panel

    Label

  • 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)  
    HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    SORBITAN ISOSTEARATE (UNII: 01S2G2C1E4)  
    TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    WATER (UNII: 059QF0KO0R)  
    WOGONIN (UNII: POK93PO28W)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    ALMOND OIL (UNII: 66YXD4DKO9)  
    SQUALANE (UNII: GW89575KF9)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71893-101-10113 g in 1 TUBE; Type 0: Not a Combination Product01/27/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34801/27/2020
    Labeler - G2 Products LLC (080963729)