Label: ARTHRITIS RELIEF CREAM- 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 20, 2021

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  • Active Ingredient section

     Menthol, Unspecified Form   1.25%

  • Purpose

    Topical Analgesic

  • Uses

    Temporarily relieves minor aches and pains of muscles and joints associated with:
    • Simple backache
    • Arthritis
    • Strains
    • Bruises
    • Sprains

  • Warnings

    For external use only.

    Do not use

    • On wounds or damaged skin

    When using this product
    • Avoid contact with eyes or mucous membranes
    • Do not bandage tightly

    Stop use and ask a doctor if
    • Condition worsens or symptoms persist for more than 7 days
    • Symptoms clear up and occur again within a few days

  • Keep out of reach of children.

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

  • Directions

    • Adults and children 12 years of age and older: Apply to affected area not more than 3 to 4 times daily.
    • Children under 12 years of age: Consult a physician.

  • Other Information.

    Questions? Need to refill? 1-800-895-2108

  • Inactive Ingredients

    Aloe Vera Gel, Cetyl Alcohol, Cetyl Esters (proprietary blend of esterified fatty acids), Cinnamon Oil, Eucalyptus Oil, Glyceryl Stearate, Grape Seed Oil, Hypromellose, Jojoba Oil, Olive Oil, Peppermint Oil, Phenoxyethanol, Potassium Sorbate, Purified Water, Sodium Benzoate, Squalane, Stearic Acid, Stearyl Alcohol, Tea Tree Oil, Vegetable Glycerin, Wintergreen Oil.

  • Product Image

    image description

  • INGREDIENTS AND APPEARANCE
    ARTHRITIS RELIEF CREAM 
    menthol cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50972-275
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM12.5 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    CETYL ESTERS WAX (UNII: D072FFP9GU)  
    CINNAMON OIL (UNII: E5GY4I6YCZ)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    GRAPE SEED OIL (UNII: 930MLC8XGG)  
    HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
    JOJOBA OIL (UNII: 724GKU717M)  
    OLIVE OIL (UNII: 6UYK2W1W1E)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    WATER (UNII: 059QF0KO0R)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SQUALANE (UNII: GW89575KF9)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    METHYL SALICYLATE (UNII: LAV5U5022Y)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50972-275-0157 mL in 1 TUBE; Type 0: Not a Combination Product10/04/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34810/04/2017
    Labeler - NewMarket Health Products LLC (055293706)
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