Label: TUSSY ANTIPERSPIRANT AND DEODORANT ORIGINAL FRESH SPICE- aluminum chlorohydrate liquid

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

Drug Label Information

Updated January 3, 2024

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  • ACTIVE INGREDIENT

    Active Ingredients                                     Purpose

    Aluminum Chlorohydrate 19%                Antiperspirant

  • PURPOSE

    Use reduces underarm perspiration

  • Use

    reduce underarm perspiration

  • WARNINGS

    Warnings For external use only

  • ASK DOCTOR

    Ask a doctor before use - if you have kidney disease

  • WHEN USING

    When using this product - do not use on broken skin - stop use if rash or irritation occurs

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

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

  • DOSAGE & ADMINISTRATION

    Directions

    Shake well and apply evenly to underarms only

    Use daily as needed

  • INACTIVE INGREDIENT

    Inactive Ingredients

    Water, PEG-40 Stearate, Cetyl Alcohol,

    Isodecyl Oleate, Mineral Oil, Magnesium Aluminum Silicate, Glyceryl Stearate,

    Methylparaben, Fragrance, Propylparaben, Trisodium HEDTA, Sorbic Acid

  • PRINCIPAL DISPLAY PANEL

    New and Improved
    Tussy
    Antiperspirant and Deodorant

    Original Fresh Spice
    pH Balanced
    1.7 FL. OZ (50.2 mL)

  • PRINCIPAL DISPLAY PANEL

    TussyAntiperspirant1.7oz

  • INGREDIENTS AND APPEARANCE
    TUSSY ANTIPERSPIRANT AND DEODORANT ORIGINAL FRESH SPICE 
    aluminum chlorohydrate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50481-3201
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE190 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    TRISODIUM HEDTA (UNII: K3E0U7O8KI)  
    SORBIC ACID (UNII: X045WJ989B)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50481-3201-150.2 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product01/27/2010
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01901/27/2010
    Labeler - KCM Brands LLC (833150472)
    Registrant - Active Creations LLC (119119545)
    Establishment
    NameAddressID/FEIBusiness Operations
    Active Creations LLC119119545manufacture(50481-3201)
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