ROLL ON ANTI-PERSPIRANT DEODORANT (ALUMINUM CHLOROHYDRATE) SOLUTION [KEEFE GROUP]

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ROLL ON ANTI-PERSPIRANT DEODORANT (ALUMINUM CHLOROHYDRATE) SOLUTION [KEEFE GROUP]
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NDC 51870-001-03
Set ID 9a1bd5aa-8720-42fe-a157-d06d122a893c
Category HUMAN OTC DRUG LABEL
Packager Keefe Group
Generic Name
Product Class
Product Number
Application Number PART350
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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Aluminum Chlorohydrate, 14% – Anhydrous Basis

  • 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

  • SPL UNCLASSIFIED SECTION

    Distributed by:
    Olivette Products, L.L.C., Bridgeton, MO 63044

  • PRINCIPAL DISPLAY PANEL - 88 ml Bottle Label

    FORCE

    POWER UP
    ANTI-PERSPIRANT
    & DEODORANT ROLL-ON

    3 fl oz/88 ml 

    PRINCIPAL DISPLAY PANEL - 88 ml Bottle Label

  • INGREDIENTS AND APPEARANCE
    ROLL ON ANTI-PERSPIRANT DEODORANT 
    aluminum chlorohydrate solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51870-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (ALUMINUM CHLOROHYDRATE - UNII:HPN8MZW13M) ALUMINUM CHLOROHYDRATE14 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)  
    Glycerin (UNII: PDC6A3C0OX)  
    Polysorbate 20 (UNII: 7T1F30V5YH)  
    Edetate Sodium (UNII: MP1J8420LU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:51870-001-0388 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product06/26/2012
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH FINALpart35006/26/2012
    Labeler - Keefe Group (839439601)
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