Label: BAN ROLL-ON ANTIPERSPIRANT DEODORANT FRESH COTTON- aluminum chlorohydrate liquid

  • NDC Code(s): 10596-340-35, 10596-340-70
  • Packager: Kao USA Inc.
  • 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 March 28, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredient

    Aluminum chlorohydrate 18%

  • PURPOSE

    Purpose

    Antiperspirant

  • INDICATIONS & USAGE

    Use

    reduces underarm perspiration

  • WARNINGS

    Warnings

    For external use only

  • DO NOT USE

    Do not use on broken skin

  • STOP USE

    Stop use if rash or irritation occurs

  • ASK DOCTOR

    Ask a doctor before use if you have kidney disease

  • 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 underarms only

  • STORAGE AND HANDLING

    Other information

    store at room temperature

  • INACTIVE INGREDIENT

    Inactive ingredients

    water, PPG-11 stearyl ether, steareth-2, steareth-20, fragrance, disodium EDTA, helianthus annuus (sunflower) seed oil, phellodendron amurense bark extract, hordeum distichon (barley) extract, santalum album (sandalwood) extract

  • SPL UNCLASSIFIED SECTION

    Questions? 1-866-226-3363

    www.bandeodorant.com

    BAN is a trademark of Kao Corp.

    Dist. by Kao USA Inc. Cincinnati, OH 45214

    ©2021 Made in Canada

  • PRINCIPAL DISPLAY PANEL

    ban

    fresh cotton
    INVISIBLE ROLL-ON

    CRUELTY FREE • PARABEN FREE • DYE FREE

    antiperspirant deodorant

    3.5 FL OZ (103 mL)

    10595-340-35-UPDATED

  • INGREDIENTS AND APPEARANCE
    BAN  ROLL-ON ANTIPERSPIRANT DEODORANT FRESH COTTON
    aluminum chlorohydrate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10596-340
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE20 g  in 103 mL
    Inactive Ingredients
    Ingredient NameStrength
    PPG-11 STEARYL ETHER (UNII: S4G2J0Y0LG)  
    WATER (UNII: 059QF0KO0R)  
    STEARETH-2 (UNII: V56DFE46J5)  
    STEARETH-20 (UNII: L0Q8IK9E08)  
    SANDALWOOD (UNII: 3641YW25N2)  
    PHELLODENDRON AMURENSE BARK (UNII: PBG27B754G)  
    BARLEY (UNII: 5PWM7YLI7R)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10596-340-35103 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product01/01/2012
    2NDC:10596-340-702 in 1 PACKAGE12/12/2019
    2103 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35001/01/2012
    Labeler - Kao USA Inc. (004251617)
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