Label: CARPE ANTIPERSPIRANT UNDERARM BERGAMOT SCENT- aluminum sesquichlorohydrate lotion

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated November 3, 2021

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  • ACTIVE INGREDIENT

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

    Anti-perspirant

    Use

    • Reduces underarm 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

    • Apply to underarms only
    • Rotate knob to dispense product and rub in vigorously 
    • For best results, apply every night before bed and again in the morning
  • Inactive ingredients

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

  • Questions?

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  • PRINCIPAL DISPLAY PANEL

    PDP 50ml

  • INGREDIENTS AND APPEARANCE
    CARPE ANTIPERSPIRANT UNDERARM BERGAMOT SCENT 
    aluminum sesquichlorohydrate lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52261-4709
    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:52261-4709-10.050 kg in 1 TUBE; Type 0: Not a Combination Product09/01/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35009/01/2021
    Labeler - Cosco International, Inc. (016433141)
    Registrant - Cosco International, Inc. (016433141)
    Establishment
    NameAddressID/FEIBusiness Operations
    Cosco International, Inc.016433141manufacture(52261-4709) , label(52261-4709) , pack(52261-4709)
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