Label: EQUATE COOL AND HEAT PAIN RELIEVING LIQUID- cool and heat pain relief liquid

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

Drug Label Information

Updated December 22, 2023

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  • DOSAGE & ADMINISTRATION

    Adults and children over 12 yrs of age: apply to the affected area no more than 3 to 4 times daily

    IF MEDICINE COMES IN CONTACT WITH HANDS, WASH WITH SOAP AND WATER.

    Children 12 years or younger: ask a doctor.

  • WARNINGS

    When using this product: use only as directed. Do not bandage tightly or use with a heating pad. Avoid contact with eyes and mucous membranes. Do not apply to wounds or damaged, broken or irritated skin. A temporary burning sensation may occur after use but normally disappears in several days. If severe burning sensation occurs, discontinue use immediately. If swelling or blistering of the skin occurs, stop use and seek medical attention. Do not expose treated area to heat or direct sunlight.

  • INACTIVE INGREDIENT

    Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Capsaicin, Glycerin, Isopropyl Myristate, Propylene Glycol, SD Alcohol 40 (30%Z), Triethanolamine, Purified Water.

  • INDICATIONS & USAGE

    Temporarily relieves minor muscle and joint pain associated with arthritis, simple backache, muscle strains, sprains, bruises.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • PURPOSE

    Topical analgesic

  • ACTIVE INGREDIENT

    Menthol 16%

  • PREGNANCY OR BREAST FEEDING

    If pregnant or breast feeding, ask a healthcare professional before use.

  • PRINCIPAL DISPLAY PANEL

    EQ CoolHeat IFC 052021.jpg.jpgEQ Cool Heat Lbl 052021.jpg.jpgEquateCoolHeatIFC.jpgEquateCoolHeatLbl.jpg.jpg

  • INGREDIENTS AND APPEARANCE
    EQUATE COOL AND HEAT PAIN RELIEVING LIQUID 
    cool and heat pain relief liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79903-006
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL16 mg  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    (C10-C30)ALKYL METHACRYLATE ESTER (UNII: XH2FQZ38D8)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    ALCOHOL (UNII: 3K9958V90M)  
    CAPSAICIN (UNII: S07O44R1ZM)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79903-006-9774 mL in 1 CONTAINER; Type 0: Not a Combination Product08/17/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01708/17/2020
    Labeler - Walmart, Inc. (051957769)
    Registrant - Pharma Nobis, LLC (118564114)
    Establishment
    NameAddressID/FEIBusiness Operations
    Pharma Nobis, LLC118564114label(79903-006) , pack(79903-006) , analysis(79903-006) , manufacture(79903-006)
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