FDA.reportPublic FDA data

Dove Soothing Chamomile Dry Spray Antiperspirant

Manufacturer
Conopco Inc. d/b/a Unilever
Effective date
2020-09-30
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:30:44

Label at a glance#

ProductDove Soothing Chamomile Antiperspirant
Active ingredientALUMINUM CHLOROHYDRATE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Aluminum chlorohydrate (20.2%)

OTC - PURPOSE SECTION

Purpose

anti-perspirant

INDICATIONS & USAGE SECTION

Uses
· reduces underarm wetness

WARNINGS SECTION

WARNINGS:• FLAMMABLE.  DO NOT USE NEAR HEAT, FLAME OR WHILE SMOKING.  CAN CAUSE SERIOUS INJURY OR DEATH.
• Keep away from face and mouth to avoid breathing in.
• Avoid spraying in eyes. Contents under pressure. Do not puncture or incinerate. Do not expose to heat or store at temperatures above 120  F/50°C or in enclosed places that could overheat.
• Do not use on broken skin. Stop use if rash or irritation occurs.
• Ask a doctor before using if you have kidney disease.
• USE ONLY AS DIRECTED.  INTENTIONAL MISUSE BY DELIBERATELY CONCENTRATING  AND INHALING THE CONTENTS CAN BE HARMFUL OR FATAL. Help stop inhalation abuse.  For information visit www.inhalant.org

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

• KEEP OUT OF REACH OF CHILDREN

DOSAGE & ADMINISTRATION SECTION

Directions

apply to underarms only

INACTIVE INGREDIENT SECTION

Inactive ingredients

Butane, Hydrofluorocarbon 152a, Cyclopentasiloxane, Isobutane, PPG-14 Butyl Ether, Fragrance (Parfum), Helianthus Annuus (Sunflower) Seed Oil, Disteardimonium Hectorite, C12-15 Alkyl Benzoate, Propane, BHT,  Octyldodecanol, Propylene Carbonate, Dimethiconol, Tocopheryl Acetate.

OTC - QUESTIONS SECTION

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

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64942-1413-12025-01-30C16284748780-19d75b9d1-1200-f424-e053-dadaa90a57ceDove Soothing Chamomile Dry Spray Antiperspirant
64942-1413-12020-09-30C16284748780-19d75b9d1-1200-f424-e053-dadaa90a57ceDove Soothing Chamomile Dry Spray Antiperspirant
64942-1413-12020-01-31C16284748780-19d75b9d1-1200-f424-e053-dadaa90a57ceDove Soothing Chamomile Dry Spray Antiperspirant

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-1413-1DoveSoothing Chamomile Antiperspirant107 g in 1 CANAEROSOL, SPRAY1073

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-1413DOVE SOOTHING CHAMOMILE ANTIPERSPIRANT (ALUMINUM CHLOROHYDRATE) AEROSOL, SPRAY [CONOPCO INC. D/B/A UNILEVER]3Legacy NDC, 1 package rows20201001_d59d7b74-df6d-4a9f-a966-8de79ed408fb.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64942-141364942-1413-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
BUTANE6LV4FOR43RIACT
1,1-DIFLUOROETHANE0B1U8K2ME0IACT
CYCLOMETHICONE 50THT5PCI0RIACT
ISOBUTANEBXR49TP611IACT
PPG-14 BUTYL ETHERR199TJT95TIACT
SUNFLOWER OIL3W1JG795YIIACT
DISTEARDIMONIUM HECTORITEX687XDK09LIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
PROPANET75W9911L6IACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
OCTYLDODECANOL461N1O614YIACT
PROPYLENE CARBONATE8D08K3S51EIACT
DIMETHICONOL (40 CST)343C7U75XWIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB

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
b0884158-20e8-e1d3-e053-2995a90a5369d59d7b74-df6d-4a9f-a966-8de79ed408fb2020-09-30WarningsExact identifier
spl id: b0884158-20e8-e1d3-e053-2995a90a5369
spl set id: d59d7b74-df6d-4a9f-a966-8de79ed408fb

Reported adverse events (FAERS/openFDA)#

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