Label: ON DUTY UNSCENTED ROLL-ON ANTI-PERSPIRANT DEODORANT- aluminum chlorohydrate gel

  • 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 January 1, 2019

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

View All Sections
  • ACTIVE INGREDIENT

    Active ingredient

    Aluminum Chlorohydrate 20.7%, anhydrous........

    Purpose

    ........Antiperspirant

  • INDICATIONS & USAGE

    Uses

    • reduces underarm perspiration
    • lasts 24 hours
  • WARNINGS

    Warnings

    For external use only

    When using this product

    • do not apply to broken skin
    • stop use if rash or irritation develops

    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.

  • DOSAGE & ADMINISTRATION

    Directions

    • apply to underarms only
  • INACTIVE INGREDIENT

    Inactive ingredients

    Water/Eau, PPG-15 Stearyl Ether, Steareth-2, Diisopropyl Adipate, Steareth-20.

  • QUESTIONS

    Questions?

    Call 1-800-FOR-AVON or 1-800-265-AVON in Canada

  • PRINCIPAL DISPLAY PANEL

    image of labelimage of DFBimage of DFBimage of DFB

  • INGREDIENTS AND APPEARANCE
    ON DUTY UNSCENTED  ROLL-ON ANTI-PERSPIRANT DEODORANT
    aluminum chlorohydrate gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10096-5219
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE207 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10096-5219-150 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product11/16/2012
    2NDC:10096-5219-275 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product11/16/2012
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35011/16/2012
    Labeler - New Avon LLC (080143520)
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!