FDA.reportPublic FDA data

Dove

Manufacturer
Conopco Inc. d/b/a/ Unilever
Effective date
2024-10-24
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:30:00

Label at a glance#

ProductDove
Active ingredientALUMINUM SESQUICHLOROHYDRATE
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 Sesquichlorohydrate (12.15 %)

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 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), Cyclopentasiloxane, C12-15 Alkyl Benzoate, Synthetic Wax, Glycerin, Calcium Chloride, Cetyl PEG/PPG-10/1 Dimethicone, Glycine, Fragrance (Parfum), Helianthus Annuus (Sunflower) Seed Oil

Questions?

OTC - QUESTIONS SECTION

Call toll-free 1-800-761-3683

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Dove Ultimate Jasmine Vanilla AP Deo ISDove Ultimate Jasmine Vanilla AP Deo IS

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
30b0ac6e-02aa-0e5c-0d8b-cffdf3a282b2Product name520250304
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
87711080-88eb-65c5-b2dd-bf99e700a372Product name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-1920-1Dove74 g in 1 CONTAINERSTICK743

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-1920DOVE (ULTIMATE JASMINE AND VANILLA 48H ANTIPERSPIRANT DEODORANT) STICK [CONOPCO INC. D/B/A/ UNILEVER]3Current NDC, Legacy NDC, 1 package rows20241027_c8a7e655-698c-32e4-e053-2995a90a76ed.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
64942-192064942-1920-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
SYNTHETIC WAX (1200 MW)Q3Z4BCH099IACT
GLYCINETE7660XO1CIACT
GLYCERINPDC6A3C0OXIACT
CYCLOMETHICONE 50THT5PCI0RIACT
ALUMINUM SESQUICHLOROHYDRATEUCN889409VACTIB
SUNFLOWER OIL3W1JG795YIIACT
CALCIUM CHLORIDEM4I0D6VV5MIACT
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 2)V2W71V8T0XIACT

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
DoveULTIMATE JASMINE AND VANILLA 48H ANTIPERSPIRANT DEODORANTConopco Inc. d/b/a/ Unileverc8a7e655-698c-32e4-e053-2995a90a76ed2024-10-24WarningsExact identifier
ndc (package): 64942-1920-1
ndc (product): 64942-1920
ndc11 (package): 64942192001
spl id: 253c65d9-3db5-5d68-e063-6394a90a0834
spl set id: c8a7e655-698c-32e4-e053-2995a90a76ed

Reported adverse events (FAERS/openFDA)#

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