BAMA FREEZE (MENTHOL) LINIMENT [JONATHAN INTERNATIONAL, INC.]

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BAMA FREEZE (MENTHOL) LINIMENT [JONATHAN INTERNATIONAL, INC.]
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NDC 70065-213-01, 70065-213-02, 70065-213-03
Set ID c1a95312-fe88-4a61-a55b-c226c9c587a3
Category HUMAN OTC DRUG LABEL
Packager Jonathan International, Inc.
Generic Name
Product Class
Product Number
Application Number PART348
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  • Drug Facts

    Active Ingredients

    Natural Menthol USP, 3.7%

  • Purpose

    Topical Analgesic

  • Keep out of reach of children

    KEEP AWAY FROM CHILDREN

  • Uses

    A deep-healing, penetrating liniment utilizing the benefits of Aloe Vera, BAMA FREEZE is excellent for temporary relief of minor aches & pains. Used for muscle and joint pains associated with arthritis, bachache, strains, sprains, etc. Just put it on the pain.

  • WARNING:

    FOR EXTERNAL USE ONLY

  • Do not use

    • on sensitive or damaged skin
    • on cuts, wounds, or with bandages
    • immediately after a shower or use of a heating pad
    • if pregnant or breasr feeding (consult a physician)
  • Directions

    Adults and children 2 years of age and older, apply liberally and rub to affected area 3-4 times daily as needed. For children under 2 years of age consult physician. Wash hands after applying. Store at 68086 degrees with lid tightly closed.

  • Inactive Ingredients

    Aloe Barbadenis leaf extractArnica Extract, Camphor, Carbomer, Ethylhexylglycerin, Ilex Paraguariensis Leaf Extract, Isopropyl Alcohol, Phenoxyethanol, Tea Tree Oil, Tocopheryl Acetate (Vitamin E Acetate), Triethanolamine, water

  • BAMA Freeze product label

    NDC 70065-213-01

    BAMA Freeze

    TOPICAL ANALGESIC

    PENETRATING ARTHRITIS RELIEF

    Put it on the pain...

    4 Fl. Oz (120 ml)

    J-Pharma Limited

    dba Jonathan International Group

    Houston, TX 77042

    U.S.A.

    www.jpharma.net

    855-667-4220

    JonInt BAMAFreeze label

  • INGREDIENTS AND APPEARANCE
    BAMA FREEZE 
    menthol liniment
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70065-213
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL3.7 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    CAMPHOR (NATURAL) (UNII: N20HL7Q941)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ARNICA MONTANA (UNII: O80TY208ZW)  
    CARBOMER 940 (UNII: 4Q93RCW27E)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70065-213-01120 mL in 1 BOTTLE; Type 0: Not a Combination Product09/01/2015
    2NDC:70065-213-0290 mL in 1 BOTTLE; Type 0: Not a Combination Product09/01/2015
    3NDC:70065-213-033785 mL in 1 JUG; Type 0: Not a Combination Product09/01/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34809/01/2015
    Labeler - Jonathan International, Inc. (809624679)
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