Label: TIDL FULL BODY PAIN RELIEF CRYOTHERAPY SPRAY.- full body pain relief cryotherapy spray. liquid

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

Drug Label Information

Updated December 4, 2023

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  • Active Ingredient

    Menthol 10.5%

  • Purpose

    Topical Analgesic

  • Use

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

  • Warnings

    For external use only

  • Do not use

    While smoking or near heat or flame

  • When Using

    ·avoid contact with the eyes or mucous membranes
    ·do not apply to wounds or damaged skin
    ·do not apply to irritated skin
    ·do not bandage
    ·wash hands after use with cool water
    ·do not use with heating pad or device

  • Stop Use

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

  • Ask Doctor

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

  • Keep Oot 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 than 3 to 4 times daily
    ·Children under 12 years of age：Consult physician

  • Inactive ingredients

    Alcohol Denat, Arnica Montana Flower Extract, Beta-Caryophyllene（Clove）, Calendula Officinalis Flower Extract, Camellia Sinensis Leaf Extract, Chamomile Recutita Flower Extract, Dimethyl Sulfone, Echinacea Angustifolia Extract, Ilex Paraguariensis Leaf Extract, Isopropyl Myristate, Juniperus Communis Fruit Extract, Oil of Wintergreen, Vanilla Extract, Water

  • Questions

    Phone：1（888）778-2986

  • PRINCIPAL DISPLAY PANEL

    1

  • INGREDIENTS AND APPEARANCE
    TIDL FULL BODY PAIN RELIEF CRYOTHERAPY SPRAY. 
    full body pain relief cryotherapy spray. liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79740-012
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL10.5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    JUNIPER BERRY (UNII: O84B5194RL)  
    CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
    ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    CHAMOMILE (UNII: FGL3685T2X)  
    ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)  
    VANILLA (UNII: Q74T35078H)  
    METHYL SALICYLATE (UNII: LAV5U5022Y)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    WATER (UNII: 059QF0KO0R)  
    CARYOPHYLLENE (UNII: BHW853AU9H)  
    ALCOHOL (UNII: 3K9958V90M)  
    ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
    DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79740-012-0190 mL in 1 BOTTLE; Type 0: Not a Combination Product12/03/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01712/03/2023
    Labeler - The Anthos Group, Inc (117511051)
    Establishment
    NameAddressID/FEIBusiness Operations
    The Anthos Group, Inc117511051manufacture(79740-012) , label(79740-012)
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