ROLL ON ANTI-PERSPIRANT (ALCOHOL FREE) (ALUMINUM CHLOROHYDRATE) SOLUTION [MCKESSON MEDICAL-SURGICAL, INC.]

ROLL ON ANTI-PERSPIRANT (ALCOHOL FREE) (ALUMINUM CHLOROHYDRATE) SOLUTION [MCKESSON MEDICAL-SURGICAL, INC.]
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NDC 68599-2303-1
Set ID a8b2aed8-dd0a-44c7-a03c-3ae00df411f5
Category HUMAN OTC DRUG LABEL
Packager McKesson Medical-Surgical, Inc.
Generic Name
Product Class
Product Number
Application Number PART350
  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Aluminum Chlorohydrate, Anhydrous Basis 10%

  • 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

    Apply to underarms only.

  • Inactive ingredients

    Purified Water, Hydroxyethylcellulose, Glycerin, Polysorbate 20, Fragrance, Tetrasodium EDTA

  • PRINCIPAL DISPLAY PANEL 

    McKESSON

    Medi-Pak

    Anti-Perspirant

    Deodorant

    Roll-On


    • Fresh Scent 


    • Protects Against

    Odor and

    Wetness



    Alcohol Free

    1.5 fl. oz. (44 ml)

    23-DR15 each

  • INGREDIENTS AND APPEARANCE
    ROLL ON ANTI-PERSPIRANT (ALCOHOL FREE) 
    aluminum chlorohydrate solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68599-2303
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE0.1 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%) (UNII: S38J6RZN16)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:68599-2303-145 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product10/19/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35008/05/2013
    Labeler - McKesson Medical-Surgical, Inc. (023904428)

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