FDA.reportPublic FDA data

Dove Men plus Care

Manufacturer
Conopco, Inc. d/b/a Unilever
Effective date
2024-11-08
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 00:35:54

Label at a glance#

ProductDove Men plus Care Clean Comfort Antiperspirant and Deodorant
Active ingredientALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Aluminum Zirconium Tetrachlorohydrex GLY (15.2%)

OTC - PURPOSE SECTION

Purpose
anti-perspirant

INDICATIONS & USAGE SECTION

Uses

· Reduces underarm wetness

· 48 hour protection

WARNINGS SECTION

Warnings
For External Use Only

OTC - DO NOT USE SECTION

Do not use on broken skin

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have kidney disease

OTC - STOP USE SECTION

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

DOSAGE & ADMINISTRATION SECTION

Directions
Apply to underarms only

INACTIVE INGREDIENT SECTION

Inactive ingredients
Cyclopentasiloxane, Stearyl Alcohol, C12-15 Alkyl Benzoate, PPG-14 Butyl Ether, Hydrogenated Castor Oil, PEF-8, Fragrance (Parfum), Dimethicone, Polyethylene, Helianthus Annuus (Sunflower) Seed Oil, Steareth-100, BHT.

OTC - QUESTIONS SECTION

Questions or comments? Call toll free 1-800-761-3683

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-1819-1Dove Men plus CareClean Comfort Antiperspirant and Deodorant76 g in 1 CONTAINERSTICK767
64942-1819-2Dove Men plus CareClean Comfort Antiperspirant and Deodorant48 g in 1 CONTAINERSTICK487
64942-1819-3Dove Men plus CareClean Comfort Antiperspirant and Deodorant14 g in 1 CONTAINERSTICK147
64942-1819-4Dove Men plus CareClean Comfort Antiperspirant and Deodorant2 in 1 PACKAGESTICK27
64942-1819-5Dove Men plus CareClean Comfort Antiperspirant and Deodorant2 in 1 PACKAGESTICK27

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-1819DOVE MEN PLUS CARE CLEAN COMFORT ANTIPERSPIRANT AND DEODORANT (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY) STICK [CONOPCO, INC. D/B/A UNILEVER]7Current NDC, Legacy NDC, 5 package rows20241109_b3fe42b0-77dc-889e-e053-2995a90a0b2e.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64942-181964942-1819-1, 64942-1819-4, 64942-1819-5, 64942-1819-2, 64942-1819-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY8O386558JEACTIB
CYCLOMETHICONE 50THT5PCI0RIACT
STEARYL ALCOHOL2KR89I4H1YIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
PPG-14 BUTYL ETHERR199TJT95TIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
POLYETHYLENE GLYCOL 400B697894SGQIACT
DIMETHICONE92RU3N3Y1OIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
HIGH DENSITY POLYETHYLENEUG00KM4WR7IACT
SUNFLOWER OIL3W1JG795YIIACT
STEARETH-1004OH5W9UM87IACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT

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
Dove Men plus Care Clean Comfort Antiperspirant and DeodorantALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLYConopco, Inc. d/b/a Unileverb3fe42b0-77dc-889e-e053-2995a90a0b2e2024-11-08WarningsExact identifier
ndc (package): 64942-1819-3
ndc (package): 64942-1819-5
ndc (package): 64942-1819-1
ndc (package): 64942-1819-4
ndc (package): 64942-1819-2
ndc (product): 64942-1819
ndc11 (package): 64942181904
ndc11 (package): 64942181905
ndc11 (package): 64942181903
ndc11 (package): 64942181901
ndc11 (package): 64942181902
spl id: 266951f8-ea54-533b-e063-6394a90a1872
spl set id: b3fe42b0-77dc-889e-e053-2995a90a0b2e

Reported adverse events (FAERS/openFDA)#

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