Label: DUKE MIDNIGHT SWIM ANTIPERSPIRANT- aluminum zirconium trichlorohydrex gly stick

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

Drug Label Information

Updated January 17, 2024

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

View All Sections
  • ACTIVE INGREDIENT

    active ingredients

  • PURPOSE

    purpose

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of children

  • INDICATIONS & USAGE

    indications & usage

  • INACTIVE INGREDIENT

    inactive ingredients

  • DOSAGE & ADMINISTRATION

    dosage & administration

  • WARNINGS

    warnings

  • PRINCIPAL DISPLAY PANEL

    package label principal

  • INGREDIENTS AND APPEARANCE
    DUKE MIDNIGHT SWIM ANTIPERSPIRANT 
    aluminum zirconium trichlorohydrex gly stick
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:60717-908
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY (UNII: T27D6T99LH) (ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY - UNII:T27D6T99LH) ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY0.2 g
    Inactive Ingredients
    Ingredient NameStrength
    POLYGLYCERIN-3 (UNII: 4A0NCJ6RD6)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)  
    DIMETHICONOL (40 CST) (UNII: 343C7U75XW)  
    ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Product Characteristics
    ColorgrayScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:60717-908-851 in 1 CANISTER; Type 0: Not a Combination Product05/09/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01905/09/2023
    Labeler - RNA PHARMA, LLC (079103999)
    Establishment
    NameAddressID/FEIBusiness Operations
    RNA PHARMA, LLC079103999manufacture(60717-908)
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!