FDA.reportPublic FDA data

equate ANTIPERSPIRANT

Manufacturer
Wal-mart Stores, Inc.
Effective date
2018-10-22
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:57:04

Label at a glance#

Productequate ANTIPERSPIRANT
Active ingredientALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Label structure9 sections

Indications and uses

• reduces underarm wetness • extra effective

Dosage and administration

• apply to underarms only • apply 2 strokes under each arm • apply to underarms at bedtime

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Zirconium Tetrachlorohydrex gly 20% (anhydrous)

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Uses

INDICATIONS & USAGE SECTION

• reduces underarm wetness • extra effective

Warnings

WARNINGS SECTION

For external use only.

Do not use on broken skin. Ask doctor before use if you have kidney disease. Stop use and ask doctor if rash or irritation occurs.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. 

Directions

DOSAGE & ADMINISTRATION SECTION

• apply to underarms only • apply 2 strokes under each arm • apply to underarms at bedtime

Inactive ingredients

INACTIVE INGREDIENT SECTION

cyclopentasiloxane, dimethicone crosspolymer, hydrogenated castor oil, dimethicone, aluminum starch octenylsuccinate, fragrance, polyethylene

SPL UNCLASSIFIED SECTION

Compare to Degree 5 &1 Clinical Strength Active Ingredient*

Clinical Strength

ANTIPERISPERANT/DEODORANT

Soft-Solid formula

Prescription strength protection against wetness

Hypoallergenic

PARABEN AND TALC FREE

20% aluminum zirconium tetrachlorohydrex GLY

Distributed by: Wal-Mart Stores, Inc., Bentonville, AR 72716, © Wal-Mart Stores, Inc.

*This product is not manufactured by Unilever, owner of the registered trademark Degree®.   GN

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
49035-146-012020-01-31C16284748780-19d75b9cf-e111-f424-e053-dadaa90a57ceEquate ANTIPERSPIRANT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49035-146-01equate ANTIPERSPIRANT48 g in 1 CANISTERSTICK482
49035-146-01equate ANTIPERSPIRANT1 in 1 BOXSTICK12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49035-146EQUATE ANTIPERSPIRANT (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY) STICK [WAL-MART STORES, INC.]2Legacy NDC, 2 package rows20181023_71998aa8-8694-44e6-bd44-d73556accc4f.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49035-14649035-146-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY8O386558JEACTIB
CYCLOMETHICONE 50THT5PCI0RIACT
DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE)UF7620L1W6IACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
DIMETHICONE92RU3N3Y1OIACT
ALUMINUM STARCH OCTENYLSUCCINATEI9PJ0O6294IACT
LOW DENSITY POLYETHYLENEJ245LN42AIIACT

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
0cfd8270-ded2-4cd3-b4ca-e68e0704c91f71998aa8-8694-44e6-bd44-d73556accc4f2018-10-22WarningsExact identifier
spl id: 0cfd8270-ded2-4cd3-b4ca-e68e0704c91f
spl set id: 71998aa8-8694-44e6-bd44-d73556accc4f

Reported adverse events (FAERS/openFDA)#

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