Label: DRY ORIGINAL FRESH 3.5OZ- aluminum chlorohydrate aerosol, spray

  • NDC Code(s): 72119-006-01
  • Packager: BLUE SEA AEROSOL & DAILY CARE CO., LTD.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 13, 2023

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  • Active ingredient

    Aluminum Chlorohydrate 20.2%

  • Purpose

    Antiperspirant

  • Uses

    Reduces underarm wetness

  • Warnings

    Flammable. Do not use near heat, flame or while smoking. Can cause serious injury or death

    Do not use

    Do not use on broken or irritated skin. Stop use if rash or irritation develops.

    When using

    • Keep away from face and mouth to avoid breathing in
    • Avoid spraying in eyes. Contents under pressure. Do not puncture or incinerate. Do not expose to heat or store at temperatures above 120ºF/50ºC or enclosed places that could overheat.
    • USE ONLY AS DIRECTED. INTENTIONAL MISUSE BY DELIBERATELY CONCENTRATING AND INHALING THE CONTENT CAN BE HARMFUL OR FATAL.

    Ask a doctor

    Ask a doctor before using, if you have kidney disease.

    Keep out of reach of children

    Keep out of reach of children

  • Directions

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

  • Inactive ingredients

    Cyclopentasiloxane; Butane; Propane; Isobutane; Hydrofluorocarbon 152A; PPG-14 Butyl Ether; C12-15 Alkyl Benzoate; Helianthus Annuus (Sunflower) Seed Oil; Fragrance; BHT; Dimethiconol; Disteardimonium Hectorite; Octldodecanol; Propylene Carbonate

  • label

    label 1

    label 2

  • INGREDIENTS AND APPEARANCE
    DRY ORIGINAL FRESH 3.5OZ 
    aluminum chlorohydrate aerosol, spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72119-006
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE20.2 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    BUTANE (UNII: 6LV4FOR43R)  
    PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    PROPANE (UNII: T75W9911L6)  
    1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)  
    PPG-14 BUTYL ETHER (UNII: R199TJT95T)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
    ISOBUTANE (UNII: BXR49TP611)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    OCTYLDODECANOL (UNII: 461N1O614Y)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72119-006-0199 g in 1 CAN; Type 0: Not a Combination Product12/13/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01912/13/2023
    Labeler - BLUE SEA AEROSOL & DAILY CARE CO., LTD. (544373091)
    Establishment
    NameAddressID/FEIBusiness Operations
    BLUE SEA AEROSOL & DAILY CARE CO., LTD.544373091manufacture(72119-006)
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