Label: ITS YOU ANTIPERSPIRANT ROLL-ON DEODORANT- aluminum sesquichlorohydrate emulsion

  • 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 February 26, 2021

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  • ACTIVE INGREDIENT

    Active Ingredient Purpose
    Aluminum sesquichlorohydrate 13.60% Antiperspirant

  • PURPOSE

    Uses

    • Reduces underarm perspiration
  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical Help or contact a Poison Control Center right away.

  • INDICATIONS & USAGE

    Stop use if rash or irritation occurs

  • WARNINGS

    Warnings
    For external use only
    Do not use on broken skin
    Ask a doctor before use if you have kidney disease

  • DOSAGE & ADMINISTRATION

    Directions

    • Apply to underarms only.
  • INACTIVE INGREDIENT

    Inactive ingredients: WATER, STEARETH-2, PPG-15 STEARYL ETHER, STEARETH-21, CYCLOHEXASILOXANE, FRAGRANCE, DICAPRYLYL CARBONATE, BENZYL ALCOHOL, 2-METHYL 5-CYCLOHEXYLPENTANOL, HYDROXYACETOPHENONE, TETRASODIUM EDTA, BISABOLOL, HEXYL CINNAMAL, LINALOOL, LIMONENE, BUTYLPHENYL METHYLPROPIONAL, CITRONELLOL, COUMARIN, GERANIOL, CITRAL.

  • PRINCIPAL DISPLAY PANEL

    It's you

    Antiperspirant roll-on Deodorant

    esika

    1.6 fl. oz. (50 ml)

    Its you antiperspirant

  • INGREDIENTS AND APPEARANCE
    ITS YOU ANTIPERSPIRANT ROLL-ON DEODORANT 
    aluminum sesquichlorohydrate emulsion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43596-0200
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALUMINUM SESQUICHLOROHYDRATE (UNII: UCN889409V) (ALUMINUM SESQUICHLOROHYDRATE - UNII:UCN889409V) ALUMINUM SESQUICHLOROHYDRATE13.6 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    COUMARIN (UNII: A4VZ22K1WT)  
    GERANIOL (UNII: L837108USY)  
    PPG-15 STEARYL ETHER (UNII: 1II18XLS1L)  
    .ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)  
    STEARETH-21 (UNII: 53J3F32P58)  
    STEARETH-2 (UNII: V56DFE46J5)  
    CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
    DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)  
    WATER (UNII: 059QF0KO0R)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    CITRAL (UNII: T7EU0O9VPP)  
    .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)  
    BUTYLPHENYL METHYLPROPIONAL (UNII: T7540GJV69)  
    LEVOMENOL (UNII: 24WE03BX2T)  
    LINALOOL, (+)- (UNII: F4VNO44C09)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:43596-0200-150 mL in 1 JAR; Type 0: Not a Combination Product03/04/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart35003/04/2021
    Labeler - Ventura Corporation LTD (602751344)
    Establishment
    NameAddressID/FEIBusiness Operations
    BEL STAR S A880160197manufacture(43596-0200)
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