Label: FAR AWAY 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 June 17, 2019

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  • ACTIVE INGREDIENT

    Active ingredient      
    Aluminum Chlorohydrate
    14.5%, 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, STEARETH-2,
    PPG-15 STEARYL ETHER,
    DICAPRYL ADIPATE, PARFUM/
    FRAGRANCE, STEARETH-20,
    ISOPROPYL PALMITATE.

  • QUESTIONS

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

  • PRINCIPAL DISPLAY PANEL

    image of PDPimage of labelimage of label

  • INGREDIENTS AND APPEARANCE
    FAR AWAY  ROLL-ON ANTI-PERSPIRANT DEODORANT
    aluminum chlorohydrate gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10096-0268
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE145 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10096-0268-150 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product02/13/2012
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35002/13/2012
    Labeler - New Avon LLC (080143520)