Label: HEMPCIN ADVANCED TOPICAL PAIN RELIEF CREAM- menthol cream

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

Drug Label Information

Updated November 5, 2023

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  • Drug Facts:

  • Active Ingredient:

    Menthol 5%

    Purpose

    Pain Relieving Cream

  • Uses:

    For the temporary relief of minor aches and pain of muscles and joints

  • Warnings:

    • For External Use only • Avoid contact with the eyes • Do not apply to wounds or damaged skin • Do not bandage tightly • Cap tube tightly and store at room temperature away from heat

    When using this product:

    • do not use in large quantities particularly over raw surfaces or blistered areas • do not exceed recommended doses unless recommended by a doctor

    Stop use and ask a doctor if:

    • allergic reaction occurs • condition worsens or does not improve within 7 days • symptoms clear up and do not return within a few days • you notice any unusual effects

    Keep out of the reach of children:

    If swallowed get medical help or call a Poison Control Center right away

  • Directions:

    • Adults or children 2 years of age and older. Apply externally to affected area not more than 3-4 times daily. • Children under 2 years of age consult a doctor

  • Other Ingredients:

    Aqua (Deionized Water), Arnica Montana Flower Extract, Boswellia Serrata Extract, Cannabis Sativa (Hemp) Seed Oil, Cassia Oil, Cetearyl Alcohol, Dimethyl Sulfone (DMSO), Ethylhexylglycerin, Glycerin, Glyceryl Stearate, Ilex Paraguariensis (Yerba Mate’) Extract, C13-14 Isoparaffin, Isopropyl Alcohol, Laureth-7, Magnesium Sulfate, Melaleuca Alternifolia (Tea Tree) Oil, Methylsulfonylmethane (MSM), PEG-100 Stearate, Phenoxyethanol, Polyacrylamide, Propylene Glycol, Sodium Polyacrylate, Stearic Acid, Triethanolamine

  • Questions:

    Call toll free 1-800-748-6539

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    HEMPCIN ADVANCED TOPICAL PAIN RELIEF CREAM 
    menthol cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51151-391
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL50 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
    INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)  
    CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)  
    CHINESE CINNAMON OIL (UNII: A4WO0626T5)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)  
    C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    LAURETH-7 (UNII: Z95S6G8201)  
    MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51151-391-001 in 1 BOX02/13/2023
    160 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01702/13/2023
    Labeler - Pedicis Research, LLC (078496974)
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