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UltraMax Roll On (Church & Dwight Co., Inc.)

Available Formats

Dosage Form Package Information Links
LIQUID 56 mL in 1 BOTTLE, WITH APPLICATOR (10237-900-19) Label Information

Complete UltraMax Roll On Information

  • Active ingredient

    Aluminum Zirconium Tetrachlorohydrex Gly (19%)


  • Purpose

    Antiperspirant


  • Use

    reduces underarm perspiration


  • Warnings For external use only

    Do not use on broken skin

    Stop use if rash or irritation occurs

    Ask a doctor before use if you have kidney disease


  • Keep out of reach of children.

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


  • Directions

    Shake well. Apply a thin layer to underarms only.


  • Inactive ingredients

    Cyclopentasiloxane, Sodium Bicarbonate (Baking Soda), Disteardimonium Hectorite, Fragrance, Propylene Carbonate, Silica, corn Starch Modified, Polysaccharides, Maltodextrin.


  • Principal Display

    Arm and Hammer
    The Standard of Purity


    ULTRA MAX
    Antiperspirant
    Deodorant


    1.9 Fl. OZ. (56mL)

    POWDER FRESH

    Carton Image UMLBF-LB19130-04-06 Carton Image


  • INGREDIENTS AND APPEARANCE
    ULTRAMAX ROLL ON  ANTIPERSPIRANT DEODORANT POWDER FRESH
    aluminum zirconium tetrachlorohydrex gly liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:10237-900
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY (UNII: 8O386558JE) (ALUMINUM CATION - UNII:3XHB1D032B) ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY 21 g  in 100 mL
    Inactive Ingredients
    Ingredient Name Strength
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    HECTORITE (UNII: 08X4KI73EZ)  
    PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:10237-900-19 56 mL in 1 BOTTLE, WITH APPLICATOR
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part350 07/28/2000
    Labeler - Church & Dwight Co., Inc. (001211952)
    Establishment
    Name Address ID/FEI Business Operations
    Church & Dwight Canada Corp 253933600 manufacture(10237-900)