Label: DZUL ARTHRITIS PAIN RELIEF- menthol cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 8, 2024

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

  • ACTIVE INGREDIENT

    Menthol 1.5%

  • PURPOSE

    Topical Analgesic

  • USE

    For the temporary relief of minor aches and pains of muscles and joints associated arthritis

  • WARNINGS

    •For external use only.

    •Ask a doctor before use if you have redness over affected area.

  • WHEN USING

    Avoid contact with the eyes or mucous membranes.
    Do not apply to wounds or damaged skin.
    Do not apply to the irritated skin or if excessive irritation develops.
    Do not bandage tightly.
    Do not use with heating pad or device.

    Stop use and ask a doctor if condition worsens, or if symptoms persist for more than 7 days, or clear up and occur again within a few days.

  • PREGNANCY OR BREAST FEEDING

    If pregnant or breast – feeding

    Ask a health professional before use.

  • KEEP OUT OF REACH OF CHILDREN

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

  • DIRECTIONS

    Adults and Children over 12 years

    Apply a small amount on the affected area.
    Massage in circular motion, let set for a few seconds.
    Repeat as necessary, but no more than 3 to 4 times daily.

    Children under 12 years of age: Do not use, consult a doctor.

  • OTHER INFORMATION

    Store tightly closed in a dry place at controlled room temperature between 59-86 F (15°-30° C).

  • INACTIVE INGREDIENT

    Water (Aqua), Paraffinum Liquidum, Alcohol Denat, Cetearyl Alcohol, Cetyl Alcohol, Stearic Acid, Dimethicone, Glyceryl Stearate, Eucalyptus Globulus Leaf Oil, Glycereth-26, Polysorbate 60, Methylsulfonylmethane (MSM), Sodium Chondroitin Sulfate, Glucosamine Sulfate, Sodium Hyaluronate, Sodium PCA, Wheat Amino Acids, Panthenol, Symphytum Officinale (Comfrey) Extract, Hydroxyproline, Acrylamide/Sodium Acrylate Copolymer, Trideceth-6, Stearyl Alcohol, Polysorbate 20, Caprylyl Glycol, Sodium Hydroxide, Phenoxyethanol, Hexylene Glycol.

  • DZUL ARTHRITIS PAIN RELIEF CREAM

    ARTHRITIS

  • INGREDIENTS AND APPEARANCE
    DZUL ARTHRITIS PAIN RELIEF 
    menthol cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83037-015
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM1.5 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
    ACRYLIC ACID/SODIUM ACRYLATE COPOLYMER (1:1; 600 MPA.S AT 0.2%) (UNII: M4PPW69Y4H)  
    AMINO ACIDS, WHEAT (UNII: 0370GZL32F)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    ALCOHOL (UNII: 3K9958V90M)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    GLYCERETH-26 (UNII: NNE56F2N14)  
    SODIUM CHONDROITIN SULFATE (PORCINE; 5500 MW) (UNII: H5BJH23Z9A)  
    GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    SYMPHYTUM OFFICINALE WHOLE (UNII: H8FJJ6KX5Y)  
    HYDROXYPROLINE (UNII: RMB44WO89X)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    TRIDECETH-6 (UNII: 3T5PCR2H0C)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83037-015-04114 g in 1 JAR; Type 0: Not a Combination Product04/20/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01704/20/2024
    Labeler - Caball Sales, Inc. (047422138)