FDA.reportPublic FDA data

Suave

Manufacturer
Conopco Inc. d/b/a Unilever
Effective date
2021-12-01
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:45:23

Label at a glance#

ProductSuave 24 Hour Fresh Antiperspirant
Active ingredientALUMINUM CHLOROHYDRATE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient:

Aluminum Chlorohydrate (19.1%)

OTC - PURPOSE SECTION

Purpose:

anti-perspirant

INDICATIONS & USAGE SECTION

Uses

· reduces underarm wetness

· 24 hour protection

WARNINGS SECTION

WARNINGS:

• FLAMMABLE UNTIL FULLY DRY.  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 degrees F/50 degrees 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, Cyclopentasiloxane, Hydrofluorocarbon 152a, Isopropyl Palmitate, Talc, Disteardimonium Hectorite, Isobutane, Propylene Carbonate, Fragrance (Parfum), Propane

OTC - QUESTIONS SECTION

Questions or comments?

Call us at 1-800-782-8301

INSTRUCTIONS FOR USE SECTION

- Shake well, hold can about six inches from underarm and spray

- Use daily for best results

- If dispenser clogs, rinse in warm water

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Suave24HrFreshAerosolPDPSuave24HrFreshAerosolPDP

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64942-1426-12023-07-28C16284748780-10191ceaa-6600-198a-e063-dbdaa90aec3eSuave 24 hour Fresh Aerosol Antiperspirant

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-1426-1Suave24 Hour Fresh Antiperspirant170 g in 1 CANAEROSOL, SPRAY1703

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-1426SUAVE 24 HOUR FRESH ANTIPERSPIRANT (ALUMINUM CHLOROHYDRATE) AEROSOL, SPRAY [CONOPCO INC. D/B/A UNILEVER]3Legacy NDC, 1 package rows20211202_eb2ee424-c064-4008-b205-2e4d9c01e65f.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64942-142664942-1426-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
BUTANE6LV4FOR43RIACT
1,1-DIFLUOROETHANE0B1U8K2ME0IACT
CYCLOMETHICONE 50THT5PCI0RIACT
ISOBUTANEBXR49TP611IACT
ISOPROPYL PALMITATE8CRQ2TH63MIACT
TALC7SEV7J4R1UIACT
DISTEARDIMONIUM HECTORITEX687XDK09LIACT
PROPANET75W9911L6IACT
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB

Source Document#

Source XML · Source PDF

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
d21a366d-ec42-7110-e053-2995a90a70dfeb2ee424-c064-4008-b205-2e4d9c01e65f2021-12-01WarningsExact identifier
spl id: d21a366d-ec42-7110-e053-2995a90a70df
spl set id: eb2ee424-c064-4008-b205-2e4d9c01e65f

Reported adverse events (FAERS/openFDA)#

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