EOUX DEODORANT

Dosage form: emulsion
Ingredients: ALUMINUM CHLOROHYDRATE 280mL in 1000mL
Labeler: SPAI SONS PHARMACEUTICAL INTERNATIONAL COSMETICS
NDC Code: 66854-009

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.

EOUX DEODORANT FOR MEN

This product is owned as a deodorant active ingredients triclosan and aluminum chlorhydroxide. Mixed effect that produced is deodorant and antiperspirant.

Eoux is an anti-bacterial and antiperspirant high protection modern biotechnical design deodorant.

This product must be keep out reach of the children.

This product is designed for use in armpit areas as may cause irritation in the area of application by the sensitivity of the user.

Hypersensivity may result in the area of application, not consume this product, if swallowed consult your doctor.

This product is topical application apply the amount necessary in desirable area and rub gently.

The design of this product does humectant agents to give best feeling in the skin effect in addition to produce antiperspirant and deodorant.

IMAGE OF THE LABEL
EOUX  DEODORANT
aluminum chlorohydrate emulsion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66854-009
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM CHLOROHYDRATE (ALUMINUM CHLOROHYDRATE) ALUMINUM CHLOROHYDRATE280 mL  in 1000 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
STEARETH-2 
CETEARETH-12 
STEARYL ALCOHOL 
POLYOXYL 20 CETOSTEARYL ETHER 
DISTEARYL ETHER 
PPG-3 MYRISTYL ETHER 
CYCLOMETHICONE 
DIMETHICONE 
DIISOPROPYL ADIPATE 
DICAPRYLYL CARBONATE 
GLYCERIN 
DIPYRITHIONE 
ALLANTOIN 
METHYLPARABEN 
PROPYLPARABEN 
TRICLOSAN 
Packaging
#Item CodePackage Description
1NDC:66854-009-0190 mL in 1 JAR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35005/31/2012
Labeler - SPAI SONS PHARMACEUTICAL INTERNATIONAL COSMETICS (880172184)
Registrant - SPAI SONS PHARMACEUTICAL INTERNATIONAL COSMETICS (880172184)
Establishment
NameAddressID/FEIOperations
SPAI SONS PHARMACEUTICAL INTERNATIONAL COSMETICS880172184analysis, label, manufacture, pack

Revised: 05/2012
 
SPAI SONS PHARMACEUTICAL INTERNATIONAL COSMETICS

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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