Label: ACUPLUS ADVANCED THERAPY FOR PAIN AND RECOVERY- menthol solution

  • NDC Code(s): 72037-136-03
  • Packager: INNOVATIONS FOR WELLNESS, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 5, 2023

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  • ​Drug Facts

  • ​Active Ingredient:

    Menthol 3.50%

    ​Purpose

    Topical Analgesic

  • ​Uses:

    Temporary relief from minor aches and pains of sore muscles & Joints associated with arthritis, simple backache, strains, bruises & sprains.

  • ​Warnings:

    Use only as directed.

    Keep out of reach of children

    For external use only. Keep away from excessive heat or flame.

    When using this product:

    Avoid contact with the eyes or mucous membranes.

    Do not apply

    • to wounds or damaged skin.
    • Do not use with other ointments, creams, sprays or liniments.
    • Do not apply to irritated skin or if excessive irritation develops
    • Do not bandage
    • Do not use with heating pad or device
    • Wash hands after use with cool water.

    Stop use and ask doctor if:

    Condition worsens, or if symptoms persist for more than 7 days.

  • ​Directions:

    ​Adults and children 2 years of age and older: ​Apply to affected area not more than three to four times daily.  ​Children under 2 years of age: ​consult a physician.  Store at room temperature.

  • ​Other Ingredients:

    Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Arnica Montana Flower Extract, Boswellia Serrata Extract, Carbomer, Cetyl Myristoleate, Ethylhexylglycerin, Glucosamine Sulfate, Glycyrrhiza Glabra (licorice) Root Extract, Ilex Paraguayensis (Yerba Mate') Extract, Isopropyl Alcohol, Magnesium Sulfate, Melaleuca Alternifolia (Tea Tree) Oil, Methylsulfonylmethane (MSM), Phenoxyethanol, Polysorbate-20, Pyridoxine HCl (Vitamin B6), Salix Alba (Willow) Bark Extract, Tetrasodium EDTA, Tocophyeryl Acetate (Vitamin E), Triethanolamine.

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    ACUPLUS ADVANCED THERAPY FOR PAIN AND RECOVERY 
    menthol solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72037-136
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL35 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
    INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)  
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    CETYL MYRISTOLEATE (UNII: 87P8K33Q5X)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)  
    LICORICE (UNII: 61ZBX54883)  
    ILEX PARAGUARIENSIS WHOLE (UNII: QJB02841ZY)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)  
    SALIX ALBA BARK (UNII: 205MXS71H7)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72037-136-0389 mL in 1 TUBE; Type 0: Not a Combination Product05/01/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01705/01/2019
    Labeler - INNOVATIONS FOR WELLNESS, LLC (051534809)
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