Label: ESIKA MAX ANTIPERSPIRANT ROLL-ON DEODORANT- aluminum sesquichlorohydrate liquid

  • 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 May 28, 2013

If you are a consumer or patient please visit this version.

View All Sections
  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Aluminum sesquichlorohydrate 13.6 %

  • Purpose

    Antiperspirant

  • Uses

    • Reduces underarm perspiration
  • Warnings

    For external use only

    Do not use on broken skin

    Ask a doctor before use if you have Kidney desease

    Stop use and ask a doctor if rash or irritation occurs

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

  • Directions

    • Apply to underarms only.
  • Inactive ingredients

    AQUA (WATER), STEARETH-2, PPG-15 STEARYL ETHER, STEARETH-21, PARFUM (FRAGRANCE), DICAPRYLYL CARBONATE, CYCLOPENTASILOXANE, CYCLOHEXASILOXANE, TRICLOCARBAN, TETRASODIUM EDTA, BENZALKONIUM CHLORIDE, BISABOLOL, MAGNESIUM NITRATE, METHYLCHLOROISOTHIAZOLIONE, MAGNESIUM CHLORIDE, METHYLISOTHIAZOLINONE.

  • SPL UNCLASSIFIED SECTION

    Dist. By Ventura Corporation, Ltd. San Juan, Puerto Rico 00926. Made in Colombia

  • PRINCIPAL DISPLAY PANEL - 50 mL Bottle Label

    MAX

    ANTIPERSPIRANT ROLL-ON
    DEODORANT
    does not contain alcohol

    ésika

    50 ml e (1.7 fl. oz.)

    Principal Display Panel - 50 mL Bottle Label
  • INGREDIENTS AND APPEARANCE
    ESIKA   MAX ANTIPERSPIRANT ROLL-ON DEODORANT
    aluminum sesquichlorohydrate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:13537-490
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Aluminum Sesquichlorohydrate (UNII: UCN889409V) (Aluminum Sesquichlorohydrate - UNII:UCN889409V) Aluminum Sesquichlorohydrate0.136 g  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    STEARETH-2 (UNII: V56DFE46J5)  
    PPG-15 STEARYL ETHER (UNII: 1II18XLS1L)  
    STEARETH-21 (UNII: 53J3F32P58)  
    DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    TRICLOSAN (UNII: 4NM5039Y5X)  
    CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    LEVOMENOL (UNII: 24WE03BX2T)  
    MAGNESIUM NITRATE (UNII: 77CBG3UN78)  
    METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
    METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:13537-490-0150 mL in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC MONOGRAPH FINALpart35005/27/2013
    Labeler - Ventura Corporation LTD. (602751344)
    Establishment
    NameAddressID/FEIBusiness Operations
    Bel Star S.A. (Colombia)880160197MANUFACTURE(13537-490)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!