Label: POWER STICK XJ COOLBLAST XTREME- aluminum sesquichlorohydrate stick

  • NDC Code(s): 42913-001-00, 42913-001-01
  • Packager: A.P. Deauville, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 3, 2023

If you are a consumer or patient please visit this version.

View All Sections
  • Active ingredient

    Aluminum Sesquichlorohydrate 20%

  • Purpose

    Antiperspirant

  • Use

    Reduces underarm wetness

  • Warnings

    For external use only

    if you have kidney disease Ask a doctor before use

    on broken skin Do not use

    rash or irritation occurs Stop use if

  • Keep out of reach of children.

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

  • Directions

    Apply to underarms only.

  • Inactive ingredients

    CYCLOPENTASILOXANE, STEARYL ALCOHOL, C12-15 ALKYL BENZOATE, PPG-14 BUTYL ETHER, TALC, HYDROGENATED CASTOR OIL, SILICA, Fragrance.

  • Questions or Comments?

     Call us at (732) 545-0200

    2011 A.P.Deauville LLC

    New Brunswick, NJ 08901

  • Power Stick XJ Coolblast Xtreme

    POWER STICK XJ Coolblast Xtreme

    Antiperspirant

    Deodorant

    NET WT. 2 OZ. (57g)

    Front

    Back

  • INGREDIENTS AND APPEARANCE
    POWER STICK XJ COOLBLAST XTREME 
    aluminum sesquichlorohydrate stick
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:42913-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM SESQUICHLOROHYDRATE (UNII: UCN889409V) (ALUMINUM SESQUICHLOROHYDRATE - UNII:UCN889409V) ALUMINUM SESQUICHLOROHYDRATE200 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    BUTYL ETHER (UNII: PBM2R52P5G)  
    TALC (UNII: 7SEV7J4R1U)  
    HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:42913-001-0057 g in 1 APPLICATOR; Type 0: Not a Combination Product11/14/2014
    2NDC:42913-001-0146 g in 1 APPLICATOR; Type 0: Not a Combination Product11/14/201405/01/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01911/14/2014
    Labeler - A.P. Deauville, LLC (118106193)
    Registrant - A.P. Deauville, LLC (118106193)
    Establishment
    NameAddressID/FEIBusiness Operations
    A.P. Deauville, LLC118106193manufacture(42913-001)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!