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Walgreens Original Antiperspirant Deodorant 2.7 oz

Dosage form: stick
Ingredients: aluminum zirconium tetrachlorohydrex gly 16.01
Labeler: VVF Kansas Services LLC
NDC Code: 10889-105

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.

Walgreens Original Powder Fresh (Aluminun Zirconium Tetrachlorohydrex Gly)

ACTIVE INGREDIENT Aluminum Zirconium Tetrachlorohydrex Gly (anhydrous) 16%




For odor protection. Reduces underarm wetness.

Turn dial to raise product. Remove plastic dome. Apply a thin even layer to underarms for maximum effectiveness.  Do not over apply.


For external use only.  Do not use on broken skin. 

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

Discontinue use if rash or irritation develops.

Keep out of reach of children.  If swallowed, get medical help or contact a poison control center right away.


Cyclopentasiloxane, Stearyl Alcohol, Talc, Dimethicone, Hydrogenated Castor Oil, Fragrance, Polyethylene, Silica, Dipropylene Glycol, Behenyl Alcohol.

* This product is not manufactured or distributed by Proctor and Gamble, owners of the registered trademark Secret (R).

Distributed by:
Walgreen Co., Deerfield, IL 60015-4616

100% Satisfaction Guaranteed

Made in USA

WIC 548698


Walgreens ORIGINAL

Anti-Perspirant and Deodorant Solid

Compare to Secret Powder Fresh*

Powder Fresh

NET WT. 2.7 OZ. (76g)

aluminum zirconium tetrachlorohydrex gly stick
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10889-105
Route of AdministrationCUTANEOUSDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
aluminum zirconium tetrachlorohydrex gly (aluminum cation) aluminum zirconium tetrachlorohydrex gly16.0 
Product Characteristics
Colorwhite (white solid) Score    
FlavorImprint Code
#Item CodePackage Description
1NDC:10889-105-131 STICK (STICK) in 1 APPLICATOR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35004/04/2008
Labeler - VVF Kansas Services LLC (791425452)
VVF Kansas Services LLC791425452manufacture

Revised: 10/2009
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.