Label: CLARISSE ANTIPERSPIRANT DEODORANRT CHERRY BLOSSOM- aluminum chlorohydrate stick

  • NDC Code(s): 76176-016-01
  • Packager: Ningbo Liyuan Daily Chemical Products Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 1, 2024

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  • Active ingredient

    Aluminum Chlorohydrate 20%

  • Purpose

    antiperspirant

  • Use

    reduces underarm wetness

  • Warnings

    For external use only

  • Do not use

    on broken or irritated skin

  • Ask a doctor before use

    if you have kidney disease

  • Stop use and ask a doctor

    if irritation or rash develops

  • Keep out of reach of children.

    If swallowed, seek medical help or contact a Poison Control Center immediately.

  • Directions

    apply to underarms only

  • Inactive ingredients

    mineral oil, stearic acid, stearyl alcohol, zea mays (corn) starch, zinc palmitate, cyclopentasiloxane, hydrogenated castor oil, fragrance, PPG-14 butyl ether, PEG-8 distearate, butylated hydroxytoluene

  • PRINCIPAL DISPLAY PANEL

    printing

  • INGREDIENTS AND APPEARANCE
    CLARISSE ANTIPERSPIRANT DEODORANRT CHERRY BLOSSOM 
    aluminum chlorohydrate stick
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:76176-016
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE20 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    PEG-8 DISTEARATE (UNII: 7JNC8VN07M)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    ZINC PALMITATE (UNII: Q7407964JA)  
    PPG-14 BUTYL ETHER (UNII: R199TJT95T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:76176-016-0145 g in 1 APPLICATOR; Type 0: Not a Combination Product01/01/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01901/01/2017
    Labeler - Ningbo Liyuan Daily Chemical Products Co., Ltd. (530766098)
    Registrant - Ningbo Liyuan Daily Chemical Products Co., Ltd. (530766098)
    Establishment
    NameAddressID/FEIBusiness Operations
    Ningbo Liyuan Daily Chemical Products Co., Ltd.530766098manufacture(76176-016)
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