Label: OLD SPICE FIJI DRY- aluminum chlorohydrate aerosol, spray

  • NDC Code(s): 84126-035-12
  • Packager: The Procter & Gamble Manufacturing Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 12, 2024

If you are a consumer or patient please visit this version.

View All Sections
  • 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

  • Questions?

    1-800-677-7582

  • SPL UNCLASSIFIED SECTION

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

  • PRINCIPAL DISPLAY PANEL - 122 g Can

    SIZE XL DRY SPRAY

    Old Spice ®

    FIJI

    with PALM TREE NOTES

    ANTIPERSPIRANT

    ALUMINUM CHLOROHYDRATE

    ANTIPERSPIRANT

    NET WT. 4.3 OZ (122 g)

    OS

  • INGREDIENTS AND APPEARANCE
    OLD SPICE FIJI DRY 
    aluminum chlorohydrate aerosol, spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84126-035
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE24.5 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    DIMETHICONOL (100000 CST) (UNII: OSA9UP217S)  
    BUTANE (UNII: 6LV4FOR43R)  
    1,1-DIFLUOROETHANE (UNII: 0B1U8K2ME0)  
    ALKYL (C12-15) 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:84126-035-12122 g in 1 CAN; Type 0: Not a Combination Product02/01/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01902/01/2024
    Labeler - The Procter & Gamble Manufacturing Company (004238200)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!