Label: NERVE REVERSE PAIN RELIEF- menthol cream

  • NDC Code(s): 73067-870-04
  • Packager: Pogue Medical Services
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 5, 2023

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  • Drug Facts

  • Active Ingredient:

    Menthol 4.00%

    Purpose

    Topical Analgesic

  • Use

    • 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 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 Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), l-Arginine, Biotin, Boswellia Serrata Extract, Carbomer, l-Carnitine, Ethylhexylglycerin, Eucalyptus Globulus Oil, Glyceryl Stearate, Lanolin, a-Lipoic Acid, Methylsulfonylmethane (MSM), Pantothenic Acid (Vitamin B5), Phenoxyethanol, Polysorbate-20, Riboflavin (Vitamin B2), Ricinus Comminis (Castor) Oil, SD-Alcohol 40B, Stearic Acid, Thiamine (Vitamin B1), Tocopheryl Acetate (Vitamin E), Triethanolamine.

  • Package Labeling:

    Label

  • INGREDIENTS AND APPEARANCE
    NERVE REVERSE PAIN RELIEF 
    menthol cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73067-870
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL40 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    WATER (UNII: 059QF0KO0R)  
    ARGININE (UNII: 94ZLA3W45F)  
    BIOTIN (UNII: 6SO6U10H04)  
    INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)  
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    LEVOCARNITINE (UNII: 0G389FZZ9M)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    LANOLIN (UNII: 7EV65EAW6H)  
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
    PANTOTHENIC ACID (UNII: 19F5HK2737)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    RIBOFLAVIN (UNII: TLM2976OFR)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73067-870-04118 mL in 1 JAR; Type 0: Not a Combination Product04/15/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01704/15/2019
    Labeler - Pogue Medical Services (085490789)
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