Label: ANTI-PERSPIRANT DEODORANT- aluminum chlorohydrate spray

  • NDC Code(s): 68599-2304-1, 68599-2304-2
  • Packager: McKesson Medical-Surgical Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 16, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Aluminum Chlorohydrate, Anhydrous Basis 13%

  • Purpose

    Antiperspirant

  • Use

    Reduces underarm wetness.

  • Warnings

    FOR EXTERNAL USE ONLY.

    KEEP OUT OF REACH OF CHILDREN.

    Do not use on broken skin.

    Stop use if rash or irritation occurs.

    Ask a doctor before use if you have kidney disease. If swallowed, get medical help or contact a Poison Control Center immediately. Use only as directed.

  • Directions

    Hold two inches from underarm and spray. Use daily for best results.

  • Inactive ingredients

    Purified Water, Isopropyl Alcohol, Propylene Glycol, Peg-40 Hydrogenated Castor Oil, Fragrance

  • PRINCIPAL DISPLAY PANEL - 59 mL Bottle Label

    McKESSON

    Anti-Perspirant

    Deodorant

    Spray

    Fresh Scent

    •

    Single Patient use

    2 fl. oz. (59 ml)

    23-H7509 each

  • INGREDIENTS AND APPEARANCE
    ANTI-PERSPIRANT DEODORANT 
    aluminum chlorohydrate spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68599-2304
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE130 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68599-2304-159 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product10/19/2017
    2NDC:68599-2304-2118 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product10/19/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01910/09/2013
    Labeler - McKesson Medical-Surgical Inc. (023904428)
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