Label: CARPE ANTIPERSPIRANT HAND WHITE JASMINE SCENT- aluminum sesquichlorohydrate lotion

  • NDC Code(s): 52261-4729-1
  • Packager: Cosco International, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 27, 2023

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  • ACTIVE INGREDIENT

    Active Ingredient                                                      Purpose
    Aluminum Sesquicholorhydrate 15% .......................Anti-perspirant

    Anti-perspirant

    Use

    • Reduces perspiration
  • Warnings

    For external use only

  • Do not use

    • on broken or irritated skin
  • Stop use and ask a doctor if

    • rash or irritation occurs

    Ask doctor before use if

    • you have kidney disease
  • Keep out of reach of children

    • If swallowed, get medical help or contact a Poison Control Center right away
  • Directions

    • Wash and dry hands throughly before application
    • Apply a small, pea-sized amount of Carpe to palms
    • Rub palms together vigorously for 15 seconds
    • For best results, apply every night before bed and an additional two times per day for at least four weeks
  • Inactive ingredients

    Aqua (Water), C12-15 Alkyl Benzoate, Citric Acid, Dimethicone, Ethylhexylglycerin, Fragrance, Glycerin, Hydroxypropyl Methylcellulose, Isopropyl Alcohol, Isopropyl Myristate, Phenoxyethanol, Polysorbate-20, Silica, Silica Silylate, Sodium Hydroxide, Talc     

  • SPL UNCLASSIFIED SECTION

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  • PRINCIPAL DISPLAY PANEL

    40ml label
  • INGREDIENTS AND APPEARANCE
    CARPE ANTIPERSPIRANT HAND WHITE JASMINE SCENT 
    aluminum sesquichlorohydrate lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52261-4729
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Aluminum Sesquichlorohydrate (UNII: UCN889409V) (ALUMINUM SESQUICHLOROHYDRATE - UNII:UCN889409V) Aluminum Sesquichlorohydrate0.15 kg  in 1 kg
    Inactive Ingredients
    Ingredient NameStrength
    water (UNII: 059QF0KO0R)  
    isopropyl alcohol (UNII: ND2M416302)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    HEXAMETHYLDISILAZANE (UNII: H36C68P1BH)  
    talc (UNII: 7SEV7J4R1U)  
    polysorbate 20 (UNII: 7T1F30V5YH)  
    dimethicone 350 (UNII: 2Y53S6ATLU)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    phenoxyethanol (UNII: HIE492ZZ3T)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    glycerin (UNII: PDC6A3C0OX)  
    HYPROMELLOSE 2208 (100000 MPA.S) (UNII: VM7F0B23ZI)  
    sodium hydroxide (UNII: 55X04QC32I)  
    citric acid monohydrate (UNII: 2968PHW8QP)  
    ethylhexylglycerin (UNII: 147D247K3P)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52261-4729-10.04738 kg in 1 TUBE; Type 0: Not a Combination Product03/01/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM35003/01/2023
    Labeler - Cosco International, Inc. (016433141)
    Registrant - Cosco International, Inc. (016433141)
    Establishment
    NameAddressID/FEIBusiness Operations
    Cosco International, Inc.016433141manufacture(52261-4729) , label(52261-4729) , pack(52261-4729)
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