FDA.reportPublic FDA data

Dove

Manufacturer
Conopco Inc. d/b/a/ Unilever
Effective date
2024-10-24
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:29:52

Label at a glance#

ProductDove
Active ingredientALUMINUM CHLOROHYDRATE
Label structure11 sections

Indications and uses

• reduces underarm wetness • 24 hour protection

Dosage and administration

apply to underarms only

Label contents#

Full prescribing information#

DOVE POWDER ROLL-ON ANTIPERSPIRANT DEODORANT - aluminum chlorohydrate liquid

DESCRIPTION SECTION

Dove Powder Roll-On AntiPerspirant Deodorant

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Aluminum Chlorohydrate (22.0%)

Purpose

OTC - PURPOSE SECTION

antiperspirant

Uses

INDICATIONS & USAGE SECTION

• reduces underarm wetness
• 24 hour protection

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

Water (Aqua), PPG-11 Stearyl Ether, Steareth-2, Steareth-20, Fragrance (Parfum), Glycerin.

Questions?

OTC - QUESTIONS SECTION

Call toll-free 1-800-761-3683

INSTRUCTIONS FOR USE SECTION

• Shake well with cap on
• Apply to underarms
• Replace cap

Package

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DovePowderAPDeoDovePowderAPDeo

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64942-1578-12020-10-30C16284748780-19d75b9d0-5119-f424-e053-dadaa90a57ceDove Powder Roll-On Antiperspirant Deodorant
64942-1578-12020-01-31C16284748780-19d75b9d0-5119-f424-e053-dadaa90a57ceDove Powder Roll-On Antiperspirant Deodorant

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-1578-1Dove74 mL in 1 CONTAINERLIQUID745

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-1578DOVE (POWDER ROLL-ON ANTIPERSPIRANT DEODORANT) LIQUID [CONOPCO INC. D/B/A/ UNILEVER]5Current NDC, Legacy NDC, 1 package rows20241027_69749de7-cae0-f339-e053-2a91aa0a3339.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
64942-157864942-1578-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
PPG-11 STEARYL ETHERS4G2J0Y0LGIACT
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB
STEARETH-20L0Q8IK9E08IACT
GLYCERINPDC6A3C0OXIACT
STEARETH-2V56DFE46J5IACT

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
DovePOWDER ROLL-ON ANTIPERSPIRANT DEODORANTConopco Inc. d/b/a/ Unilever69749de7-cae0-f339-e053-2a91aa0a33392024-10-24WarningsExact identifier
ndc (package): 64942-1578-1
ndc (product): 64942-1578
ndc11 (package): 64942157801
spl id: 253bd708-f288-aecc-e063-6294a90a382d
spl set id: 69749de7-cae0-f339-e053-2a91aa0a3339

Reported adverse events (FAERS/openFDA)#

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