Lacura Extreme Blast anti-perspirant deodorant

Dosage form: stick
Ingredients: ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY 250mg in 1g
Labeler: VVF Kansas Services LLC
NDC Code: 10889-110

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.

Lacura Extreme Blast (Aluminun Zirconium Trichlorohydrex Gly)

ACTIVE INGREDIENT Aluminum Zirconium Trichlorohydrex Gly 20%

PURPOSE

Anti-perspirant

USES

Reduces underarm wetness.

WARNINGS

For external use only. 

Do not use on broken skin. 

Ask a doctor before you use if you have kidney disease.

Stop use if rash or irritation occurs.

Keep out of reach of children.

If swallowed get medical help or contact a Poison Control Center immediately.




Directions

Apply evenly to underarms only.

Do not store over 115 degrees F

Inactive IngredientsCyclopentasiloxane, Stearyl Alcohol, PPG-14 Butyl Ether, Hydrogenated Castor  Oil, Zinc Ricinoleate, Fragrance, Talc, PEG-8 Distearate.

Distributed By:

ALDI INC.
BATAVIA, IL
60510
(MI01.89CT)

100% Satisfaction Guaranteed
www.ALDI.us

If swallowed, get medical help or contact a Poison Control Center immediately.




Lacura

For Men
Extreme Blast
Antiperspirant +Deodorant
Lasting Protection
Invisible Stick

NET WT. 2.7OZ (76g)
LACURA EXTREME BLAST  ANTI-PERSPIRANT DEODORANT
aluminum zirconium trichlorohydrex gly stick
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10889-110
Route of AdministrationCUTANEOUSDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY (ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY) ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY250 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
Stearyl Alcohol 
PPG-14 Butyl Ether 
Hydrogenated Castor Oil 
Zinc Ricinoleate 
Talc 
PEG-8 Distearate 
Product Characteristics
Colorwhite (white solid) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:10889-110-1776 g in 1 PACKAGE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35012/13/2010
Labeler - VVF Kansas Services LLC (791425452)
Establishment
NameAddressID/FEIOperations
VVF Kansas Services LLC791425452manufacture

Revised: 11/2010
 
VVF Kansas Services LLC

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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