Walgreens Original

Manufacturer
VVF Kansas Services LLC
Effective date
2009-10-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:22:39

Label at a glance#

ProductWalgreens Original Antiperspirant Deodorant 2.7 oz
Active ingredientaluminum zirconium tetrachlorohydrex gly
Label structure7 sections

Indications and uses

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.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Aluminum Zirconium Tetrachlorohydrex Gly (anhydrous) 16%

PURPOSE

OTC - PURPOSE SECTION

Anti-perspirant

USES

INDICATIONS & USAGE SECTION

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.

WARNINGS

WARNINGS AND PRECAUTIONS SECTION

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.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

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

SPL UNCLASSIFIED SECTION

* 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  www.walgreens.com

Made in USA

WIC 548698

PRODUCT LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Walgreens ORIGINAL

Anti-Perspirant and Deodorant Solid

Compare to Secret Powder Fresh*

Powder Fresh

NET WT. 2.7 OZ. (76g)WalgreensOriginalLabelWalgreensOriginalLabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10889-105-132019-10-21C16284748780-1956f9ecf-d92f-621f-e053-dbdaa90a74adWalgreens Original Powder Fresh (Aluminun Zirconium Tetrachlorohydrex Gly)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10889-105-13Walgreens OriginalAntiperspirant Deodorant 2.7 oz1 in 1 APPLICATORSTICK11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10889-105WALGREENS ORIGINAL ANTIPERSPIRANT DEODORANT 2.7 OZ (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY) STICK [VVF KANSAS SERVICES LLC]1Legacy NDC, 1 package rows20091026_454a03ff-f652-410a-830b-5ba3caf5f8d9.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
aluminum zirconium tetrachlorohydrex glyACTIVE INGREDIENT8O386558JE1
aluminum cationACTIVE MOIETY3XHB1D032B1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10889-10510889-105-13

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 1 matching rows.

Name, UNII, Kind table
NameUNIIKind
aluminum zirconium tetrachlorohydrex gly8O386558JEACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
454a03ff-f652-410a-830b-5ba3caf5f8d9454a03ff-f652-410a-830b-5ba3caf5f8d92009-10-23WarningsExact identifier
spl id: 454a03ff-f652-410a-830b-5ba3caf5f8d9
spl set id: 454a03ff-f652-410a-830b-5ba3caf5f8d9

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.