FDA.reportPublic FDA data

Dove

Manufacturer
Conopco Inc. d/b/a/ Unilever
Effective date
2024-11-06
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:34:37

Label at a glance#

ProductDove
Active ingredientALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Label structure9 sections

Indications and uses

• reduces underarm wetness

Dosage and administration

apply to underarms only

Label contents#

Full prescribing information#

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Aluminum Zirconium Tetrachlorohydrex GLY (11.4 %)

Purpose

OTC - PURPOSE SECTION

antiperspirant

Uses

INDICATIONS & USAGE SECTION

• reduces underarm wetness

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Cyclopentasiloxane, Stearyl Alcohol, C12-15 Alkyl Benzoate, PPG-14 Butyl Ether, Hydrogenated Castor Oil, PEG-8, Dimethicone, Hydroxystearic Acid, Fragrance (Parfum), Polyethylene, Silica, Helianthus Annuus (Sunflower) Seed Oil, Steareth-100, BHT, Niacinamide, Alpha-Isomethyl Ionone, Benzyl Alcohol, Benzyl Salicylate, Citronellol, Geraniol. Hexyl Cinnamal, Limonene, Linalool.

Questions?

OTC - QUESTIONS SECTION

Call 1-800-761-3683

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Dove Rosewood AP ISDove Rosewood AP IS

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-2136-1Dove74 g in 1 CONTAINERSTICK742

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-2136DOVE (EVEN TONE PLUS NIACINAMIDE ROSEWOOD AND POWDER ANTIPERSPIRANT DEODORANT) STICK [CONOPCO INC. D/B/A/ UNILEVER]2Current NDC, 1 package rows20241108_0035ae96-13dd-9cac-e063-6394a90addea.zip

Products#

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

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64942-213664942-2136-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZYL SALICYLATEWAO5MNK9TUIACT
LINALOOL, (+/-)-D81QY6I88EIACT
.BETA.-CITRONELLOL, (R)-P01OUT964KIACT
ISOMETHYL-.ALPHA.-IONONE9XP4LC555BIACT
BENZYL ALCOHOLLKG8494WBHIACT
.ALPHA.-HEXYLCINNAMALDEHYDE7X6O37OK2IIACT
LIMONENE, (+)-GFD7C86Q1WIACT
CYCLOMETHICONE 50THT5PCI0RIACT
STEARYL ALCOHOL2KR89I4H1YIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
HIGH DENSITY POLYETHYLENEUG00KM4WR7IACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY8O386558JEACTIB
PPG-14 BUTYL ETHERR199TJT95TIACT
SUNFLOWER OIL3W1JG795YIIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
DIMETHICONE92RU3N3Y1OIACT
STEARETH-1004OH5W9UM87IACT
POLYETHYLENE GLYCOL 400B697894SGQIACT
NIACINAMIDE25X51I8RD4IACT
12-HYDROXYSTEARIC ACID933ANU3H2SIACT
GERANIOLL837108USYIACT

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
DoveEVEN TONE PLUS NIACINAMIDE ROSEWOOD AND POWDER ANTIPERSPIRANT DEODORANTConopco Inc. d/b/a/ Unilever0035ae96-13dd-9cac-e063-6394a90addea2024-11-06WarningsExact identifier
ndc (package): 64942-2136-1
ndc (product): 64942-2136
ndc11 (package): 64942213601
spl id: 2645202a-0708-849d-e063-6294a90a166b
spl set id: 0035ae96-13dd-9cac-e063-6394a90addea

Reported adverse events (FAERS/openFDA)#

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