CYZONE  XPRESS YOUR BODY- aluminum sesquichlorohydrate liquid 
Ventura Corporation LTD.

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.

----------

CYZONE XPRESS YOUR BODY
Clarity

Información del medicamento

Ingredientes activos

Aluminum sesquichlorohydrate 20%

Propósito

Antitranspirante

Uso

Advertencias

  • No usar en piel dañada o lastimada

  • Consulte con el doctor en caso de sufrir de enfermedad renal

  • Detenga su uso y consulte al doctor si sucede enrojecimiento

  • Mantener fuera del alcance de los niños. Si es ingerido obtener ayuda médica o contactar al centro de Control de Envenenamiento inmediatamente

Instrucciones

Ingredientes inactivos

Aqua (water), steareth-2, steareth-21, ppg-15 stearyl ether, cyclopentasiloxane, propylene glycol, cyclohexasiloxane, parfum (fragrance), sodium lactate, dicaprylyl carbonate, butylene glycol, triclosan, arctostaphylos uva ursi leaf extract, methylparaben, bisabolol, benzalkonium chloride, bht, serica (silk), tetrasodium edta, rosa gallica flower extract.

PR: Distributed by Ventura Corporation, Ltd. San Juan, Puerto Rico 00926.

PRINCIPAL DISPLAY PANEL - 50 ml Bottle Label

xpress
your body

Clarity

desodorante
antitranspirante
para una piel con
apariencia más clara

50 ml e (1.6 fl.oz)

cy°zone

PRINCIPAL DISPLAY PANEL - 50 ml Bottle Label
CYZONE   XPRESS YOUR BODY
aluminum sesquichlorohydrate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:13537-430
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Aluminum Sesquichlorohydrate (UNII: UCN889409V) (Aluminum Sesquichlorohydrate - UNII:UCN889409V) Aluminum Sesquichlorohydrate0.2 g  in 1 mL
Inactive Ingredients
Ingredient NameStrength
water (UNII: 059QF0KO0R)  
steareth-2 (UNII: V56DFE46J5)  
steareth-21 (UNII: 53J3F32P58)  
ppg-15 stearyl ether (UNII: 1II18XLS1L)  
cyclomethicone 5 (UNII: 0THT5PCI0R)  
propylene glycol (UNII: 6DC9Q167V3)  
cyclomethicone 6 (UNII: XHK3U310BA)  
sodium lactate (UNII: TU7HW0W0QT)  
dicaprylyl carbonate (UNII: 609A3V1SUA)  
butylene glycol (UNII: 3XUS85K0RA)  
triclosan (UNII: 4NM5039Y5X)  
arctostaphylos uva-ursi leaf (UNII: 3M5V3D1X36)  
methylparaben (UNII: A2I8C7HI9T)  
levomenol (UNII: 24WE03BX2T)  
benzalkonium chloride (UNII: F5UM2KM3W7)  
butylated hydroxytoluene (UNII: 1P9D0Z171K)  
bombyx mori fiber (UNII: 6LK42KUV6W)  
edetate sodium (UNII: MP1J8420LU)  
rosa gallica flower (UNII: X8W61WUV70)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:13537-430-0150 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart35006/08/2012
Labeler - Ventura Corporation LTD. (602751344)
Establishment
NameAddressID/FEIBusiness Operations
Bel Star S.A. (Colombia)880160197MANUFACTURE(13537-430)

Revised: 7/2012
Document Id: d824f125-45f3-4096-aecc-76467482ba08
Set id: d53522a6-1b21-4f30-9767-af061d550904
Version: 1
Effective Time: 20120709
 
Ventura Corporation LTD.