Label: VANICREAM ANTI-PERSPIRANT/DEODORANT- aluminum zirconium trichlorohydrex gly stick

  • NDC Code(s): 45334-305-02
  • Packager: Pharmaceutical Specialties, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 2, 2023

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  • Drug Facts

  • ACTIVE INGREDIENT

    Active ingredient

    Aluminum zirconium trichlorohydrex gly 20% (anhydrous)

  • PURPOSE

    Purpose

    antiperspirant

  • INDICATIONS & USAGE

    Uses

    • reduces underarm wetness
    • 24 hour extra effective protection
  • WARNINGS

    Warnings

    For external use only

  • DO NOT USE

    Do not use on broken skin

  • ASK DOCTOR

    Ask a doctor before use if you have kidney disease

  • STOP USE

    Stop use if rash or irritation occurs

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

  • DOSAGE & ADMINISTRATION

    Directions

    apply to underams only

  • STORAGE AND HANDLING

    Other information

    Store at room temperature

  • INACTIVE INGREDIENT

    Inactive ingredients

    cyclopentasiloxane, hydrogenated poly(C6-14 olefin), stearyl alcohol, phenyl trimethicone, hydrogenated castor oil, cetyl alcohol, silica

  • SPL UNCLASSIFIED SECTION

    *To learn more about our products and ingredients, visit www.vanicream.com or call 1-800-325-8232.

    Dist. by PHARMACEUTICAL SPECIALTIES, INC.

    Rochester, MN 55901 U.S.A.

    Made in Canada

    Vanicream is a trademark, or registered trademark, of Pharmaceutical Specialties, Inc. in the U.S. or other countries.

    KD21A

  • PRINCIPAL DISPLAY PANEL

    NDC 45334-305-02

    DERMATOLOGIST TESTED

    VANICREAM™

    Anti-perspirant/Deodorant

    Free of dyes, fragrance, masking fragrance, lanolin, parabens & formaldehyde releasers

    FOR SENSITIVE SKIN

    Net Wt 2.25 oz (64 g)

    label

  • INGREDIENTS AND APPEARANCE
    VANICREAM ANTI-PERSPIRANT/DEODORANT 
    aluminum zirconium trichlorohydrex gly stick
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:45334-305
    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 GLY12.8 g  in 64 g
    Inactive Ingredients
    Ingredient NameStrength
    PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)  
    HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    HYDROGENATED POLY(C6-14 OLEFIN; 6 CST) (UNII: 3C785871IX)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:45334-305-0264 g in 1 CONTAINER; Type 0: Not a Combination Product11/11/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01911/11/2016
    Labeler - Pharmaceutical Specialties, Inc. (076499557)
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