Label: TIDL SPORT CRYOTHERAPY JOINT MUSCLE cream

  • NDC Code(s): 79740-008-01, 79740-008-02
  • Packager: ANTHOS GROUP, INC, THE
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 20, 2024

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  • Active Ingredient(s)

    Menthol 2%

  • Purpose

    Topical Analgesic

  • Use

    Temporary relief from minor aches and pains of muscles and joints associated with arthritis simple backache strains and sprains

  • Warnings

    Warnings For external use only.

  • Do not use

    do not use with heating pad or device.

  • STOP USE

    Stop use and ask a doctor if

    condition worsens , or if symptoms persist for more than 7 days or clear up and reoccur again within a few days.

  • WHEN USING

    When using this product

    avoid contact with the eyes or mucous membranes.

    do not apply to wounds or damaged skin.

    do not apply to the irritated skin .

    do not bandage.

    wash hands after use with cool water .

    do not use with heating pad or device.

  • KEEP OUT OF REACH OF CHILDREN

    If accidentally ingested get medical help or contact a Poison Control Center immediately

  • Directions

    Adults and children 12 years of age and older: Apply to affected area not more than3 to 4 times daily.

    Children under 12 years of age : Consult physician.

  • Other information

    /

  • Inactive ingredients

    Purified Water, Propylene Glycol USP, Organic Aloe Vera Juice, Isopropyl Myristate, Ceteareth 20, Methyl Salicylate, Eucalyptus Oil, Wintergreen Oil, Camphor Oil, Clove Bud, Beta-Caryophyllene（Clove）, Glyceryl Stearate, Phenoxyethanol, Caprylyl Glycol, Ethyloxiglycerin, Disodium EDTA, Capsaicin, Organic Azulene, Carbomer, Aminomethyl Propanol

  • Package Label - Principal Display Panel

    79740-008-0179740-008-02

  • INGREDIENTS AND APPEARANCE
    TIDL SPORT CRYOTHERAPY JOINT MUSCLE 
    tidl sport cryotherapy joint muscle cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79740-008
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL2 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    1,2-PROPANEDIOL, 1-BENZOATE (UNII: K4K90ZQ89N)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    METHYL SALICYLATE (UNII: LAV5U5022Y)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    WATER (UNII: 059QF0KO0R)  
    CLOVE (UNII: K48IKT5321)  
    CARYOPHYLLENE (UNII: BHW853AU9H)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    CAMPHOR LEAF OIL (UNII: 51D0RGY52V)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
    CAPSAICIN (UNII: S07O44R1ZM)  
    AZULENE (UNII: 82R6M9MGLP)  
    POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79740-008-0190 mL in 1 BOTTLE; Type 0: Not a Combination Product01/20/2022
    2NDC:79740-008-0290 mL in 1 BOX; Type 0: Not a Combination Product01/20/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01701/20/2022
    Labeler - ANTHOS GROUP, INC, THE (117511051)
    Establishment
    NameAddressID/FEIBusiness Operations
    ANTHOS GROUP, INC, THE117511051manufacture(79740-008)
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