Label: HAIKU 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

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  • ACTIVE INGREDIENT

    Active ingredient

    Aluminum Chlorohydrate 14.5%, anhydrous......................

    ​Purpose

    ​Antiperspirant

  • INDICATIONS & USAGE

    Uses

    • reduces underarm perspiration
  • WARNINGS

    Warnings

    For external use only

    Do not use on broken skin

    Ask a doctor before use if you have kidney disease

    Stop use if rash or irritation occurs

    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

  • PRINCIPAL DISPLAY PANEL

    image of labelimage of DFB

  • INGREDIENTS AND APPEARANCE
    HAIKU  ROLL-ON ANTI-PERSPIRANT DEODORANT
    aluminum chlorohydrate gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10096-0868
    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:10096-0868-150 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product11/14/2012
    2NDC:10096-0868-275 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product11/14/2012
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35011/14/2012
    Labeler - New Avon LLC (080143520)