Cyzone Rock You

Dosage form: liquid
Ingredients: Aluminum sesquichlorohydrate 8.5g in 50mL
Labeler: Ventura Corporation Limited
NDC Code: 13537-222

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.

ROCK
YOU
cy°zone

Drug Facts

Active Ingredient

Aluminum sesquichlorohydrate 17%

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, triclosan, cyclohexasiloxane, tetrasodium edta, benzalkonium chloride, bisabolol, magnesium nitrate, methylchloroisothiazolinone, magnesium chloride, methylisothiazolinone.

Questions?

Puerto Rico: 622-3235 (San José)

PRINCIPAL DISPLAY PANEL - 50 ml Bottle Label

Desodorante Antitranspirante Roll On

ROCK
YOU
cy°zone

50 ml e (1.6 fl.oz.)

CYZONE   ROCK YOU
aluminum sesquichlorohydrate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:13537-222
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Aluminum sesquichlorohydrate (Aluminum Cation) Aluminum sesquichlorohydrate8.5 g  in 50 mL
Inactive Ingredients
Ingredient NameStrength
water 
steareth-2 
steareth-21 
dicaprylyl carbonate 
cyclomethicone 5 
triclosan 
cyclomethicone 6 
edetate sodium 
benzalkonium chloride 
levomenol 
magnesium nitrate 
methylchloroisothiazolinone 
magnesium chloride 
methylisothiazolinone 
Packaging
#Item CodePackage Description
1NDC:13537-222-5050 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart35011/08/2011
Labeler - Ventura Corporation Limited (602751344)
Establishment
NameAddressID/FEIOperations
BelStar, S.A.880160197MANUFACTURE

Revised: 11/2010
 
Ventura Corporation Limited

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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