Label: THERACARE ICE BLUE GEL PAIN RELIEVING- menthol gel

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

Drug Label Information

Updated December 18, 2024

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  • Active ingredient

    Menthol 2%

  • Purpose

    Topical analgesic

  • Uses

    ● temporarily relieves minor aches and pains of muscles and joints associated with:

    ● simple backache

    ● arthritis

    ● strains

    ● bruises

    ● sprains

  • Warnings

    For external use only

  • When Using this product

    • with other topical pain relievers
    • with heating pads or heating devices
    • avoid contact with eyes
    • do not bandage tightly
    • do not apply to wounds or damage skin
  • Stop use and ask a doctor if

    • condition worsens or symptoms persist for more than 7 days or clear up and occur again within a few days
  • If pregnant or breast-feeding

    ask a health professional before use

  • Keep Out of Reach of Children

    If swallowed, get medical help or contact a Poison Control Center (800-222-1222) right away.

  • Directions

    • clean affected area before applying product
    • adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily
    • children under 2 years of age: ask a doctor before using this product
  • Other information

    • do not freeze
    • store at room temperature
    • keep container tightly closed when not in use
    • do not use, pour, spill, or store near heat or open flame
  • Inactive ingredients

    ammonium hydroxide, benzyl alcohol, carbopor 940, cupric sulfate, FD&C blue no. 1, isopropyl alcohol, magnesium sulfate, PEG-40 hydrogenated castor oil, sodium hydroxide, thymol, water

  • Questions or comments?

    Customer care 866-326-1313

  • Principal Display

    label

  • INGREDIENTS AND APPEARANCE
    THERACARE ICE BLUE GEL  PAIN RELIEVING
    menthol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71101-217
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL20 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    AMMONIA (UNII: 5138Q19F1X)  
    CARBOMER 940 (UNII: 4Q93RCW27E)  
    CUPRIC SULFATE (UNII: LRX7AJ16DT)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    THYMOL (UNII: 3J50XA376E)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71101-217-01226.8 g in 1 JAR; Type 0: Not a Combination Product01/01/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01701/01/2022
    Labeler - Veridian Healthcare (830437997)
    Establishment
    NameAddressID/FEIBusiness Operations
    ANICARE PHARMACEUTICALS PRIVATE LIMITED916837425manufacture(71101-217)
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