Label: MENTHO PATCH COOL- menthol patch

  • NDC Code(s): 72602-002-01
  • Packager: THE EGYPTIAN SAUDI CO FOR MEDICAL MANUFACTURING MASCOMID
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 19, 2023

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  • Purpose 

    For the temprorary releif of minor aches and pains of musceles and joints associated with simple backache, arthritis,strainsand sprains

  • Warnings

    • FOR EXTERNAL USE ONLY
    • When Using this Product
    • Avoid contact with eyes
    • Do not apply to open wounds, or to damaged skin
    • Do not bandage tightly.
  • Directions

    • Adults and children 3 years of age and older: apply to affected area not more than 3 to 4 times daily.
    • Children under 3 years of age: consult doctor.
  • INDICATIONS & USAGE

  • Stop use and ask doctor

    • If condition worsens
    • If symptoms persist more than 7 days or clear up and occur again with a few days
  • storage

    • store in cool dry place avoid direct sunlight.
  • KEEP OUT OF REACH OF CHILDREN

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

  • Active ingridient section

    Menthol,Camphor,Methyl salicylate

  • INACTIVE INGREDIENT SECTION

    Glycerin ,Sodium poly acryl ate ,Aluminum chloride hex hydrate 2 ,
    Anhydrous citric acid ,Tartaric acid 1 ,Poly sorbate -80 (tween 80) 0.5 ,Isopropyl myristate alcohol 2.5 ,Car boxy methyl cellulose (CMC) 2 
    EDETA 0.5 ,Polyvinyl pyrolidone(PVP-K90) 3 ,Water 48.35 ,titanium dioxide 0.05,ACRYLATE/ C10-30 ALKYL ACRYLATE,cross polymer

  • Product label

    image descriptionimage description

  • INGREDIENTS AND APPEARANCE
    MENTHO PATCH  COOL
    menthol patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72602-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL15 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)  
    ALUMINUM CHLORIDE ANHYDROUS (UNII: LIF1N9568Y)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    TARTARIC ACID (UNII: W4888I119H)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    CARBOXYMETHYLCELLULOSE SODIUM (0.9 CARBOXYMETHYL SUBSTITUTION PER SACCHARIDE; 600 MPA.S AT 2%) (UNII: ZY4732LP1O)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    POLYACRYLIC ACID (800000 MW) (UNII: D0I6NSZ87U)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    WATER (UNII: 059QF0KO0R)  
    CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72602-002-0110 g in 1 PATCH; Type 0: Not a Combination Product09/21/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01709/20/2018
    Labeler - THE EGYPTIAN SAUDI CO FOR MEDICAL MANUFACTURING MASCOMID (850486280)
    Registrant - THE EGYPTIAN SAUDI CO FOR MEDICAL MANUFACTURING MASCOMID (850486280)
    Establishment
    NameAddressID/FEIBusiness Operations
    THE EGYPTIAN SAUDI CO FOR MEDICAL MANUFACTURING MASCOMID850486280manufacture(72602-002)
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