Label: AQUAX DEO- aluminum chlorohydrate cream

  • NDC Code(s): 82160-313-01
  • Packager: Pella Pharmaceuticals Co. Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated November 25, 2021

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  • Forms and presentation

    Cream: Tube of 75 g

  • Active Ingredient

    Aluminum Chlorohydrate

  • Inactive Ingredients

    Aqua, Cetearyl Alcohol, Ceteareth-22, Glycerin, Petrolatum, Ceteareth-25, Sodium Citrate, Methylparaben, Citric Acid, Parfum, Propylparaben.

  • Purpose

    Antiperspirant

  • Properties

    Aquax ® Deo cream reduces excessive sweating (hyperhidrosis)

  • Indications

    Aquax ® Deo cream is used to reduce excessive perspiraton (hyperhidrosis)

  • Precautions

    keep out of reach of children

  • Warnings

    • For external use only
    • Do not apply to broken or irritated skin
    • Do not shave auxiliaries for 24 hours before application
  • Contraindications

    Hypersensitivity to any of the components

  • Side effects

    Aquax ® Deo cream has no known side effect, its us is without risk

  • Dosage and administration

    Dry the area to be treated, and then apply Aquax ® Deo cream at night, at bed time

  • Storage conditions

    Store at a temperature belwo 30 °C

  • Primary Package

    Primary Package

  • Secondary Package

    Secondary Package

  • INGREDIENTS AND APPEARANCE
    AQUAX DEO 
    aluminum chlorohydrate cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82160-313
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE150 mg  in 75 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    CETEARETH-22 (UNII: 28VZG1E234)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    CETEARETH-25 (UNII: 8FA93U5T67)  
    SODIUM CITRATE (UNII: 1Q73Q2JULR)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82160-313-011 in 1 CARTON03/15/2011
    175 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35003/15/2011
    Labeler - Pella Pharmaceuticals Co. Ltd (562370925)
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