FDA.reportPublic FDA data

Dove

Manufacturer
Conopco Inc. d/b/a/ Unilever
Effective date
2022-12-07
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-05-31 23:52:13

Label at a glance#

ProductDove
Active ingredientALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Label structure10 sections

Indications and uses

reduces underarm wetness 24 hour protection extra effective

Dosage and administration

apply to underarms only before bed, apply two clicks of product to each underarm

Label contents#

Full prescribing information#

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Aluminum Zirconium Tetrachlorohydrex GLY (20%)

Purpose

OTC - PURPOSE SECTION

antiperspirant

Uses

INDICATIONS & USAGE SECTION

reduces underarm wetness
24 hour protection
extra effective

Warnings

WARNINGS SECTION

• For external use only.
• Do not use on broken skin .
• Ask a doctor before use if you have kidney disease.
• Stop use 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
before bed, apply two clicks of product to each underarm

Other information

OTHER SAFETY INFORMATION

Do not store over 115°F

Inactive ingredients

INACTIVE INGREDIENT SECTION

Cyclopentasiloxane, Dimethicone, Paraffin, Microcrystalline Wax, Silica, Fragrance (Parfum), Helianthus Annuus (Sunflower) Seed Oil, Dimethicone Crosspolymer, BHT, Citronellol, Hexyl Cinnamal.

Questions?

OTC - QUESTIONS SECTION

Call toll-free 1-800-761-3683

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Dove Men Extra Fresh 76 HR AP CartonDove Men Extra Fresh 76 HR AP CartonDove Men Extra Fresh 76 HR APDove Men Extra Fresh 76 HR AP

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64942-1731-12025-01-30C16284748780-12cef2736-81b4-d83d-e063-dadaa90ab31fDove Men Clinical Protection Extra Fresh 76 HR Antiperspirant
64942-1731-22025-01-30C16284748780-12cef2736-81b4-d83d-e063-dadaa90ab31fDove Men Clinical Protection Extra Fresh 76 HR Antiperspirant

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-1731-1Dove48 g in 1 CONTAINERSTICK485
64942-1731-2Dove2 in 1 PACKAGESTICK25

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-1731DOVE (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY) STICK [CONOPCO INC. D/B/A/ UNILEVER]5Legacy NDC, 2 package rows20221208_a135f462-9d6a-ac6a-e053-2a95a90a6e83.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64942-173164942-1731-1, 64942-1731-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
CYCLOMETHICONE 50THT5PCI0RIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY8O386558JEACTIB
PARAFFINI9O0E3H2ZEIACT
DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE)UF7620L1W6IACT
SUNFLOWER OIL3W1JG795YIIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
.ALPHA.-HEXYLCINNAMALDEHYDE7X6O37OK2IIACT
DIMETHICONE92RU3N3Y1OIACT
.BETA.-CITRONELLOL, (R)-P01OUT964KIACT
MICROCRYSTALLINE WAXXOF597Q3KYIACT

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
ef40607f-fee3-828b-e053-2995a90afd70a135f462-9d6a-ac6a-e053-2a95a90a6e832022-12-07WarningsExact identifier
spl id: ef40607f-fee3-828b-e053-2995a90afd70
spl set id: a135f462-9d6a-ac6a-e053-2a95a90a6e83

Reported adverse events (FAERS/openFDA)#

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