Label: STOPAIN CLINICAL- menthol, unspecified form gel

  • NDC Code(s): 63936-9750-1, 63936-9750-2, 63936-9750-3, 63936-9750-4
  • Packager: Troy Manufacturing, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 18, 2024

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  • Drug Facts

  • Active Ingredient

    Menthol 10.0%

    Purpose

    Topical Analgesic

  • Uses

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

    • simple backache
    • arthritis
    • strains
    • bruises
    • sprains
  • Warnings

    ​Avoid contact with eyes. ​For external use only.

    Flammable: Keep away from fire or flame.

    When using this product

    • use only as directed 
    • do not bandage tightly or use a heating pad
    • do not apply to wounds or damaged skin

    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
    • redness is present 
    • excessive irritation of the skin develops

    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:

    ask a doctor.​​ ​Children 12 years or younger:

    • apply directly onto affected area without the need to bandage
    • repeat if necessary, but do not apply more than 4 times daily.
  • Other Information 

    • Store at room temperature
  • Inactive Ingredients

    acrylic acid/vinyl ester copolymer, dimethylsulfone (MSM), eucalyptus oil, glucosamine sulfate, hydroxypropylcellulose, SD alcohol 39C, PEG-8 dimethicone, pentylene glycol, peppermint oil, triethanolamine, water (USP).

  • Package Labeling:118ml

    Label5

  • Package Labeling:473ml

    Label6

  • Package Labeling:946ml

    Label

  • Package Labeling:3785ml

    Label8

  • INGREDIENTS AND APPEARANCE
    STOPAIN CLINICAL 
    menthol, unspecified form gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63936-9750
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM100 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ACRYLIC ACID (UNII: J94PBK7X8S)  
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)  
    HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)  
    PEG-8 DIMETHICONE (UNII: GIA7T764OD)  
    PENTYLENE GLYCOL (UNII: 50C1307PZG)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63936-9750-3118 mL in 1 TUBE; Type 0: Not a Combination Product01/18/2017
    2NDC:63936-9750-4473 mL in 1 BOTTLE; Type 0: Not a Combination Product01/18/2017
    3NDC:63936-9750-2946 mL in 1 BOTTLE; Type 0: Not a Combination Product01/18/2017
    4NDC:63936-9750-13785 mL in 1 BOTTLE; Type 0: Not a Combination Product01/18/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01701/18/2017
    Labeler - Troy Manufacturing, Inc. (160075248)
    Registrant - Troy Manufacturing, Inc. (160075248)
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