Label: OLD SPICE AQUA REEF DRY ANTIPERSPIRANT- aluminum chlorohydrate aerosol, spray

  • NDC Code(s): 69423-640-12
  • Packager: The Procter & Gamble Manufacturing Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 14, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Aluminum chlorohydrate 25.0% (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, fragrance, C12-15 alkyl benzoate, corn starch/maltodextrin crosspolymer,

    cyclodextrin, disteardimonium hectorite, mineral oil, triethyl citrate, dimethiconol

  • SPL UNCLASSIFIED SECTION

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

  • Questions or comments?

    1-800-677-7582

  • PRINCIPAL DISPLAY PANEL - 122 g Can

    Old Spice ®

    AQUA REEF

    ANTIPERSPIRANT

    DRY SPRAY

    24/7 LASTING

    SWEAT DEFENSE

    ALUMINUM CHLOROHYDRATE

    ANTIPERSPIRANT

    NET WT. 4.3 OZ (122 g)

    OS

  • INGREDIENTS AND APPEARANCE
    OLD SPICE AQUA REEF DRY ANTIPERSPIRANT 
    aluminum chlorohydrate aerosol, spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69423-640
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE25 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    PPG-14 BUTYL ETHER (UNII: R199TJT95T)  
    BUTANE (UNII: 6LV4FOR43R)  
    1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    DIMETHICONOL (100000 CST) (UNII: OSA9UP217S)  
    PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
    ARGAN OIL (UNII: 4V59G5UW9X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69423-640-12122 g in 1 CAN; Type 0: Not a Combination Product10/17/202206/01/2025
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01910/17/202206/01/2025
    Labeler - The Procter & Gamble Manufacturing Company (004238200)
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