Label: DURADRY PM SWEAT MINIMIZING ANTIPERSPIRANT GEL- aluminum chloride hexahydrate gel

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

Drug Label Information

Updated November 10, 2023

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  • Active ingredient

    ALUMINUM CHLORIDE (HEXAHYDRATE) 15%

  • Purpose

    Antiperspirant

  • Uses

    Reduces underarm perspiration

  • Warnings

    For external use only
    Stop use if rash or irritation occurs.

  • Do not use

    • On broken, irritated or recently shaved skin.
    • Immediately after bathing.
    • In or near eyes. If contact occurs, rise eyes thoroughly with water.
  • 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

    • Apply to underarms only.
    • Apply a small amount of product to underarms at bedtime. It may itch during initial application.
    • The next morning, rinse underarms with abundant water and apply a regular antiperspirant. For best results, use DURADRY® AM.
    • Apply DURADRY® PM for a few nights in a row or until the excessive perspiration is controlled. Then Apply twice a week or as needed for maintenance.
  • Inactive ingredients

    Aqua, Propylene Glycol, Xanthan Gum, Sodium Bicarbonate,Disodium EDTA, Salicylic Acid.

  • Questions?

    Learn more at duradry.com

    Dist. by:

    NOVADORE USA, LLC
    Miami, FL 33179

  • DURADRY PM (ALUMINUM CHLORIDE HEXAHYDRATE)

    pm-tube

    pm-pouch

  • INGREDIENTS AND APPEARANCE
    DURADRY PM SWEAT MINIMIZING ANTIPERSPIRANT GEL 
    aluminum chloride hexahydrate gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69990-102
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLORIDE (UNII: 3CYT62D3GA) (ALUMINUM CATION - UNII:3XHB1D032B) ALUMINUM CHLORIDE150 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SALICYLIC ACID (UNII: O414PZ4LPZ)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    WATER (UNII: 059QF0KO0R)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69990-102-011 in 1 POUCH02/20/2018
    110.5 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01901/01/2015
    Labeler - Novadore USA Inc (079777451)
    Registrant - Novadore USA Inc (079777451)
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