Label: SECRET ORIGINAL DRY POWDER FRESH (aluminum chlorohydrate- anhydrous aerosol, spray

  • NDC Code(s): 84126-063-11
  • Packager: The Procter & Gamble Manufacturing Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 11, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Aluminum chlorohydrate 24.5% (anhydrous)

  • Purpose

    Antiperspirant

  • Use

    • reduces underarm wetness
  • 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.

    When using this product

    keep away from face and mouth to avoid breathing it

    avoid spraying in eyes

    use only as directed; intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal

  • SAFE HANDLING WARNING

    Flammable

    do not spray near flame or while smoking

    contents under pressure
    do not crush, puncture or incinerate

    do not expose to heat or store at temperature above 120ºF

  • Directions

    • apply to underarms only
  • Inactive ingredients

    Butane, hydrofluorocarbon 152A, dimethicone, C12-15 alkyl benzoate, isopropyl myristate, PPG-14 butyl ether, fragrance, disteardimonium hectorite,mineral oil, propylene carbonate, corn starch/maltodextrin crosspolymer, dimethiconol, argania spinosa kernel oil

  • Questions?

    1-800-964-1947

  • SPL UNCLASSIFIED SECTION

    Dist. by PROCTER & GAMBLE,
    CINCINNATI, OH 45202.

  • PRINCIPAL DISPLAY PANEL - 116 g Can

    Secret ®

    ORIGINAL

    DRY SPRAY

    pH Balancing Minerals

    POWDER FRESH

    ALUMINUM CHLOROHYDRATE

    ANTIPERSPIRANT / DEODORANT

    NET WT. 4.1 OZ (116 g)

    Sec

  • INGREDIENTS AND APPEARANCE
    SECRET ORIGINAL DRY POWDER FRESH 
    aluminum chlorohydrate (anhydrous) aerosol, spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84126-063
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE ANHYDROUS (UNII: 407PSC3OC7) (ALUMINUM CHLOROHYDRATE ANHYDROUS - UNII:407PSC3OC7) ALUMINUM CHLOROHYDRATE ANHYDROUS24.5 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    DIMETHICONOL (100000 CST) (UNII: OSA9UP217S)  
    ARGANIA SPINOSA KERNEL OIL (UNII: 4V59G5UW9X)  
    BUTANE (UNII: 6LV4FOR43R)  
    HYDROFLUOROCARBON 152A (UNII: 0B1U8K2ME0)  
    C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)  
    DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
    PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    PPG-14 BUTYL ETHER (UNII: R199TJT95T)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84126-063-11116 g in 1 CAN; Type 0: Not a Combination Product01/15/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01901/15/2024
    Labeler - The Procter & Gamble Manufacturing Company (004238200)
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