Label: ARTHRITIS PAIN RELIEVING CREAM- menthol, methyl salicylate cream

  • NDC Code(s): 51367-036-75
  • Packager: International Nature Nutraceuticals, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 19, 2024

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  • Active Ingredients

    Menthol- 16%

    Methyl Salicylate- 26%

  • Uses

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

    • Simple backache
    • Sprains
    • Bruises
    • Arthritis
  • Warnings

    For external use only

  • Do not use

    • On wounds
    • On the face
    • Damaged or irritated skin
    • Otherwise than as directed
  • When using this product

    • Avoid contact with the eyes, mouth or mucous membranes
    • Do not bandage tightly
  • Stop using and consult with doctor if:

    • Condition worsens
    • Symptoms persist for more than 7 days or clear up and occur again within a few days.
    • Use with caution if you are allergic to ingredients
  • If pregnant consult a doctor before use

  • Keep out of reach of children to avoid accidental poisoning

  • Other Information

    Keep bottle tightly closed, store in a cool place

    If swallowed, get medical help or contact poison control center immediately 

  • Directions

    • Adults and children 2 years of age and older: apply to affected area not more than 3-4 times daily, children under 2 years of age: Do not use, consult a doctor
  • Inactive Ingredients

    White Petrolatum, Eucalyptus Oil, Lanolin Oil, Paraffin

  • Package

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  • INGREDIENTS AND APPEARANCE
    ARTHRITIS PAIN RELIEVING CREAM 
    menthol, methyl salicylate cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51367-036
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL12 g
    METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE19.5 g
    Inactive Ingredients
    Ingredient NameStrength
    WHITE PETROLATUM (UNII: B6E5W8RQJ4)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    LANOLIN OIL (UNII: OVV5IIJ58F)  
    PARAFFIN (UNII: I9O0E3H2ZE)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51367-036-751 in 1 BOTTLE; Type 0: Not a Combination Product08/01/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drugpart34808/01/2024
    Labeler - International Nature Nutraceuticals, Inc. (006106879)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zhejiang Dingtai Pharmaceutical Co., Ltd420598724manufacture(51367-036)
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