Label: NUTURNA ARTHRITIS INTENSIVE CONCENTRATE FOR PAIN RELIEF AND RECOVERY- menthol cream

  • NDC Code(s): 81996-244-02, 81996-244-04, 81996-244-08
  • Packager: Nuturna International LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 4, 2024

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  • Drug Facts

  • Active Ingredients

    Menthol 3.70%

    Purpose

    Topical Analgesic

  • Uses:

    • For the temporary relief of minor aches and pains of muscles and joints, associated with simple backache, arthritis, strains, bruises and sprains.
  • Warnings:

    For external use only

    Do not use

    • On damaged or broken skin.

    When using this product

    • Avoid contact with the eyes. 
    • Do not bandage tightly

    Stop use and ask a doctor if

    • Rash or irritation develops and lasts.
    • Condition worsens, or if symptoms persist for more than 7 days or clear up and occurs again within a few days.

    Keep out of reach of children.

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

    If pregnant or breast-feeding,

    ask a health professional before use.

  • 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.
    • We recommend testing a small amount of cream on your skin first to check for skin reaction and comfort level, wait 15 minutes before applying to affected area if you are happy with the comfort level.
  • Inactive ingredients:

    Aloe Barbadensis Leaf(Aloe Vera Gel)Juice, Arnica Montana Flower Extract, Carbomer, Ilex Paraguariensis (Yerba Mate) Extract, Isopropyl Alcohol, Melaleuca Alternifolia (Tea Tree) Oil, Methylisothiazolinone, Methylsulfonylmethane (MSM), Polysorbate-20, Tocopheryl Acetate (Vitamin E), Triethanolamine, FD & C Blue # 1.

  • Other information:

    • Protect the product in this container from excessive heat and direct sun.
  • Questions ?

    customerservice@nuturna.com

  • Package Labeling:57g

    Label

  • Package Labeling:114g

    Label2

  • Package Labeling:228g

    Label3

  • INGREDIENTS AND APPEARANCE
    NUTURNA ARTHRITIS INTENSIVE CONCENTRATE FOR PAIN RELIEF AND RECOVERY 
    menthol cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81996-244
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL3.7 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
    ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81996-244-0257 g in 1 JAR; Type 0: Not a Combination Product05/28/2021
    2NDC:81996-244-04114 g in 1 JAR; Type 0: Not a Combination Product05/28/2021
    3NDC:81996-244-08228 g in 1 JAR; Type 0: Not a Combination Product05/28/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01711/22/2020
    Labeler - Nuturna International LLC (117795246)
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