FDA.reportPublic FDA data

DOVE Antiperspirant

Manufacturer
All Natural Dynamics | Unilever Manufacturera S. de R.L. de C.V.
Effective date
2022-03-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:48:48

Label at a glance#

ProductDOVE Antiperspirant
Active ingredientALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Label structure12 sections

Indications and uses

reduces underarm wetness

Dosage and administration

apply to underarms only

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Zirconium Tetrachlorohydrex GLY (15.2%)

Purpose

OTC - PURPOSE SECTION

anti-perspirant

Uses

INDICATIONS & USAGE SECTION

reduces underarm wetness

Warnings

WARNINGS SECTION

· For External Use Only.

· Do not use

OTC - DO NOT USE SECTION

on broken skin.

· Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

kidney disease.

· Stop use if

OTC - STOP USE SECTION

rash or irritation occurs.

· Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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, Parfum, Dimethicone, Polyethylene, Helianthus Annuus Seed Oil, Steareth-100, BHT, Alpha-Isomethyl Ionone, Benzyl Benzoate, Benzyl Salicylate, Butylphenyl Methylpropional, Citronellol, Geraniol, Hexyl Cinnamal, Hydroxycitronellal, Linalool

Questions?

OTC - QUESTIONS SECTION

Call 1-800-761-3683

Dove Original Antiperspirant Deodorant Stick

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Original Antiperspirant Deodorant StickOriginal Antiperspirant Deodorant Stick

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51769-089-092024-01-30C16284748780-11030e365-0d79-111a-e063-dadaa90a10e2Dove Original Antiperspirant Deodorant Stick

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51769-089-09DOVE Antiperspirant40 g in 1 APPLICATORSTICK401

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51769-089DOVE ANTIPERSPIRANT (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY) STICK [ALL NATURAL DYNAMICS ]1Legacy NDC, 1 package rows20220319_da72e1a9-2d7c-1c32-e053-2a95a90a0f91.zip

Products#

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

DailyMed product names page 1 of 1 · 26 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51769-08951769-089-09

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 25 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZYL ALCOHOLLKG8494WBHIACT
BENZYL BENZOATEN863NB338GIACT
BENZYL SALICYLATEWAO5MNK9TUIACT
BUTYLPHENYL METHYLPROPIONALT7540GJV69IACT
.BETA.-CITRONELLOL, (R)-P01OUT964KIACT
GERANIOLL837108USYIACT
CYCLOMETHICONE 50THT5PCI0RIACT
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY8O386558JEACTIB
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
PPG-14 BUTYL ETHERR199TJT95TIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
HIGH DENSITY POLYETHYLENEUG00KM4WR7IACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ACONITIC ACID93371T1BXPIACT
ISOMETHYL-.ALPHA.-IONONE9XP4LC555BIACT
.ALPHA.-HEXYLCINNAMALDEHYDE7X6O37OK2IIACT
ISOEUGENOL5M0MWY797UIACT
LINALOOL, (+/-)-D81QY6I88EIACT
HYDROXYCITRONELLAL8SQ0VA4YURIACT
LIMONENE, (+)-GFD7C86Q1WIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
STEARYL ALCOHOL2KR89I4H1YIACT
DIMETHICONE92RU3N3Y1OIACT
SUNFLOWER OIL3W1JG795YIIACT
STEARETH-1004OH5W9UM87IACT

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
da72e1a9-2d7d-1c32-e053-2a95a90a0f91da72e1a9-2d7c-1c32-e053-2a95a90a0f912022-03-17WarningsExact identifier
spl id: da72e1a9-2d7d-1c32-e053-2a95a90a0f91
spl set id: da72e1a9-2d7c-1c32-e053-2a95a90a0f91

Reported adverse events (FAERS/openFDA)#

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