Label: URBAN STREET OCEAN BREEZE- ocean breeze roll on antiperspirant/deodorant stick

  • 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 July 8, 2021

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  • Active Ingredient

    Aluminum Chloride 25.0%

  • Purpose

    Antiperspirant

  • Use

    Reduces underarm perspiration. Extra effective

  • Warnings

    For external use only

    Do not use on broken skin.

    Stop use and ask a doctor if rash or irritation occurs

    Keep out of reach of children. If swallowed, get medical help or contact poison control center right away.

    Ask a doctor before use if you have kidney disease.

  • Directions

    Apply to underarms only.

  • Inactive Ingredients:

    Water, Steareth-2, Steareth-31, Fragrance, PPF-15 Stearyl Ether, Phenoxyethanol, Aluminum Starch Octenylsuccinate, Isopropyl Myristate, Methylisothiazolinone

  • INDICATIONS & USAGE

  • PRINCIPAL DISPLAY PANEL

    Urban Street Ocean BreezeUrban Street

    Ocean Breeze

    Roll On

    Antiperspirant/Deodorant

    3.25 fl. oz. (96.1 ml)

  • INGREDIENTS AND APPEARANCE
    URBAN STREET OCEAN BREEZE 
    ocean breeze roll on antiperspirant/deodorant stick
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:22431-227
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM CHLORIDE (UNII: 3CYT62D3GA) (ALUMINUM CATION - UNII:3XHB1D032B) ALUMINUM CHLORIDE250 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    STEARETH-21 (UNII: 53J3F32P58)  
    PPG-15 STEARYL ETHER (UNII: 1II18XLS1L)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF)  
    WATER (UNII: 059QF0KO0R)  
    STEARETH-2 (UNII: V56DFE46J5)  
    ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)  
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:22431-227-019.6 g in 1 TUBE; Type 0: Not a Combination Product07/19/2021
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35007/19/2021
    Labeler - Blue Cross Laboratories LLC (008298879)
    Registrant - Blue Cross Laboratories LLC (008298879)
    Establishment
    NameAddressID/FEIBusiness Operations
    Blue Cross Laboratories008298879manufacture(22431-227)
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