Label: BIOFREEZE- menthol gel

  • NDC Code(s): 59316-102-10, 59316-102-11, 59316-102-12, 59316-102-15, view more
    59316-102-16, 59316-102-20, 59316-102-25, 59316-102-28, 59316-102-30, 59316-102-40, 59316-102-50, 59316-102-80, 59316-102-90, 59316-102-91, 59316-102-92, 59316-102-98
  • Packager: RB Health (US) LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 13, 2023

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  • Drug Facts

  • Active Ingredients:


    Menthol USP 4%

    Purpose

    Pain Relieving Gel

  • Uses:

    Temporarily relieves minor aches and pains of muscles and joints associated with: • simple backache • arthritis • strains • bruises • sprains

  • Warnings:

    For external use only

    Flammable: Keep away from excessive heat or open flame

    When using this product:

    • Use only as directed • Avoid contact with the eyes or on mucous membranes • Do not apply to wounds or damaged skin • Do not apply to irritated skin or if excessive irritation develops • Do not bandage tightly or use with heating pad or device

    Stop use and ask a doctor if:

    You experience pain, swelling or blistering of the skin; condition worsens, or if symptoms persist for more than 7 days, or clear up and occur again within a few days; arthritic pain persists for more than 10 days, or redness is present, or in conditions affecting children under 12 years of age

    If pregnant or breastfeeding:

    Ask a health professional before use

    Keep out of reach of children:

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

  • Directions:

    • Adults and children 2 years of age and older:Rub a thin film over affected area not more than 3 to 4 times daily
    • Children under 2 years of age:Consult a physician
    • wash hands after use with cool water
  • Other information

    - store at 20-25°C (68-77°F) - store in a cool dry place away from direct sunlight

  • Inactive Ingredients:

    Aloe Barbadensis Leaf Extract, Arctium Lappa Root (Burdock) Extract, Arnica Montana Flower Extract, Blue 1, Boswellia Carterii Resin Extract, Calendula Officinalis Extract, Camellia Sinensis Leaf Extract, Camphor, Carbomer, Glycerin, Ilex Paraguariensis Leaf Extract, Isopropyl Alcohol, Isopropyl Myristate, Melissa Officinalis (Lemon Balm) Leaf Extract, Silica, Tocopheryl Acetate, Triethanolamine, Water, Yellow 5

  • Questions or Comments:

     1-800-246-3733

  • SPL UNCLASSIFIED SECTION

    Dist. by: RB Health (US)
    Parsippany, NJ 07054-0224

  • PRINCIPAL DISPLAY PANEL - 473 mL Bottle Label

    CLINICALLY
    RECOMMENDED ®

    NDC 59316-102-30

    BiOFREEZE ®
    COOL THE PAIN

    GEL

    MENTHOL-PAIN
    RELIEVING GEL

    16 FL OZ (1 PT) 473 mL

    PRINCIPAL DISPLAY PANEL - 473 mL Bottle Label
  • INGREDIENTS AND APPEARANCE
    BIOFREEZE 
    menthol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59316-102
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM40 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)  
    ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3)  
    FRANKINCENSE (UNII: R9XLF1R1WM)  
    CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    MELISSA OFFICINALIS LEAF (UNII: 50D2ZE9219)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    WATER (UNII: 059QF0KO0R)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59316-102-105 mL in 1 BOTTLE; Type 0: Not a Combination Product01/03/2012
    2NDC:59316-102-113 mL in 1 BOTTLE; Type 0: Not a Combination Product01/03/2012
    3NDC:59316-102-1589 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product01/03/201212/31/2018
    4NDC:59316-102-20118 mL in 1 BOTTLE; Type 0: Not a Combination Product01/03/2012
    5NDC:59316-102-25118 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product01/03/201212/31/2021
    6NDC:59316-102-30473 mL in 1 BOTTLE; Type 0: Not a Combination Product01/03/2012
    7NDC:59316-102-40946 mL in 1 BOTTLE; Type 0: Not a Combination Product01/03/2012
    8NDC:59316-102-503785 mL in 1 CONTAINER; Type 0: Not a Combination Product01/03/2012
    9NDC:59316-102-9830 mL in 1 BOTTLE; Type 0: Not a Combination Product01/03/2012
    10NDC:59316-102-8044 mL in 1 TUBE; Type 0: Not a Combination Product11/02/2018
    11NDC:59316-102-1289 mL in 1 BOTTLE; Type 0: Not a Combination Product09/19/2016
    12NDC:59316-102-1689 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product09/19/201612/31/2019
    13NDC:59316-102-28237 mL in 1 BOTTLE; Type 0: Not a Combination Product09/19/2016
    14NDC:59316-102-90100 in 1 CARTON01/03/2012
    14NDC:59316-102-105 mL in 1 BOTTLE; Type 0: Not a Combination Product
    15NDC:59316-102-9110 in 1 CARTON01/03/201212/31/2025
    15NDC:59316-102-113 mL in 1 BOTTLE; Type 0: Not a Combination Product
    16NDC:59316-102-9216 in 1 CARTON01/03/201212/31/2025
    16NDC:59316-102-113 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01701/03/2012
    Labeler - RB Health (US) LLC (081049410)
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