ZIMS MAX FREEZE PRO FORMULA- menthol, unspecified form gel

ZIMS MAX FREEZE by

Drug Labeling and Warnings

ZIMS MAX FREEZE by is a Otc medication manufactured, distributed, or labeled by KOBAYASHI Healthcare International, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

  • QUESTIONS

    Consumer Comments Call:
    1-800-432-8629

  • SPL UNCLASSIFIED SECTION

    Distributed by: KOBAYASHI
    Consumer Products, LLC

    P.O. Box 1191, Dalton, GA 30722

  • PRINCIPAL DISPLAY PANEL - 85 g Bottle Label

    EXTRA STRENGTH

    ZIM'S™
    MAX-
    FREEZE

    PRO FORMULA

    - LONGER LASTING* -
    PAIN RELIEF

    • - FAST ACTING
    • - LONG LASTING
    • - VANISHING SCENT

    COLD THERAPY
    COOLING ROLL-ON
    with 7% Menthol

    Net Wt 3oz (85g)

    *compared to original

    PRINCIPAL DISPLAY PANEL - 85 g Bottle Label
  • INGREDIENTS AND APPEARANCE
    ZIMS MAX FREEZE   PRO FORMULA
    menthol, unspecified form gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 54273-007
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM70 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ARNICA MONTANA (UNII: O80TY208ZW)  
    VANILLYL BUTYL ETHER (UNII: S2ULN37C9R)  
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    TEA TREE OIL (UNII: VIF565UC2G)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC: 54273-007-0185 g in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product08/01/2018
    2NDC: 54273-007-02102 g in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product02/01/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH NOT FINALpart34808/01/2018
    Labeler - KOBAYASHI Healthcare International, Inc. (156391729)

  • © 2022 FDA.report
    This site is not affiliated with or endorsed by the FDA.