Label: MINTED LEAF COLD THERAPY FOOT RELIEF WITH CBD AND MENTHOL- menthol gel

  • NDC Code(s): 73102-064-00
  • Packager: MMG Consumer Brands, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 13, 2024

If you are a consumer or patient please visit this version.

View All Sections
  • Drug Facts

  • Active ingredient

    Menthol 16.00%

    Purpose

    Topical Analgesic

  • Indications

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

    • For external use only.
    • Avoid contact with eyes.
    • If symptoms persist for more than seven days, discontinue use and consult physician.

    Keep out of reach of children.

    If swallowed, consult physician.

    Do not apply

    • to wounds or damaged skin.
    • Do not bandage tightly.

    If pregnant or breast feeding,

    contact physician prior to use.

  • Directions

    • Adults and children two-years of age or older: Apply to affected area not more than three to four times daily.
    • Children under two-years of age: consult a physician.
  • Additional Information

    • Store at room temperature.
  • Other Ingredients:

    Aloe Barbadensis (Aloe Vera Gel) Juice, Aqua (Deionized Water), Arnica Montana Extract, Betaglucan, Cannabis Sativa (Full Spectrum Hemp) Oil, Caprylic/Capric Triglyceride, Cetearyl Olivate, Gluconolactone, Glycerin, Glyceryl Stearate, Helianthus Annuus (Sunflower) Oil, Isopropyl Alcohol, Methylsulfonylmethane (MSM), Petrolatum, Sodium Benzoate, Sodium Polyacrylate, Sorbitan Olivate, Stearic Acid, Tocopheryl Acetate (Vitamin E), Urea, Xanthan Gum, Zemea (Corn) Propanediol.

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    MINTED LEAF COLD THERAPY FOOT RELIEF WITH CBD AND MENTHOL 
    menthol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73102-064
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL160 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    ARNICA MONTANA (UNII: O80TY208ZW)  
    CANNABIS SATIVA WHOLE (UNII: B5ONF538PB)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    CETEARYL OLIVATE (UNII: 58B69Q84JO)  
    GLUCONOLACTONE (UNII: WQ29KQ9POT)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SORBITAN OLIVATE (UNII: MDL271E3GR)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    UREA (UNII: 8W8T17847W)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73102-064-0085 g in 1 TUBE; Type 0: Not a Combination Product08/01/201901/01/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01708/01/201901/01/2023
    Labeler - MMG Consumer Brands, LLC (117036455)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!