Label: ANTIPERSPIRANT DRY 1.6 OZ LADY ANTIPERSPIRANT- aluminum chlorohydrate aerosol, spray

  • NDC Code(s): 57337-108-01
  • Packager: Rejoice International Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 28, 2024

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  • ACTIVE INGREDIENT

    Active Ingredient ........................................................................... Purpose

    Aluminum Chlorohydrate 23.3% .................................................. Antiperspirant

  • PURPOSE

    Antiperspirant

  • 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.

  • INDICATIONS & USAGE

    Reduces underarm wetness

  • WARNINGS

    Warnings

    For external use only.

    Flammable.

    Do not spray near flame or while smoking.
    Contents under pressure
    Do not crush, puncture or incinerate container.
    Do not expose to heat or store at temperatures above 120oF
    Do not use on broken skin.
    Ask a doctor before using, if you have kidney disease.
    When using this product
    Keep away from face and mouth to avoid breathing it. Avoid spraying in eyes.
    Use only directed. Intentional missuse by deliberately concentrating and inhaling the contents can be harmful or fatal
    Stop use if rash or irritation develops.

  • DOSAGE & ADMINISTRATION

    Directions

    • For underarm use only. Shake can well before each use. Hold can 6 inches away from skin. Spray underarm.
  • INACTIVE INGREDIENT

    Inactive Ingredients

    Isobutane, Butane, Hydrofluorocarbon 152a, Cyclopentasiloxane, Ethyl Alcohol, PPG-14 Butyl Ether, Helianthus Annuus Seed Oil, Isopropryl Myristate, C12-15 Alkyl Benzoate, Frangrance, Propane, Aluminum Starch Ocetenylsuccinate, Disteardimonium Hectorite, Dimethicone, Tocopheryl Acetate, BHT, Silica

  • PRINCIPAL DISPLAY PANEL

    Label

  • INGREDIENTS AND APPEARANCE
    ANTIPERSPIRANT DRY 1.6 OZ LADY  ANTIPERSPIRANT
    aluminum chlorohydrate aerosol, spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57337-108
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE23.3 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    ISOBUTANE (UNII: BXR49TP611)  
    1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    PROPANE (UNII: T75W9911L6)  
    LAURYL PHOSPHATE (UNII: 0K08L8GE2H)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)  
    DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    PPG-14 BUTYL ETHER (UNII: R199TJT95T)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:57337-108-0145 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product01/13/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01901/13/2020
    Labeler - Rejoice International Inc. (078741245)
    Establishment
    NameAddressID/FEIBusiness Operations
    BLUE SEA AEROSOL & DAILY CARE CO., LTD.544373091manufacture(57337-108)