FDA.reportPublic FDA data

Suave Coconut Kiss 48HR Protection Dry Spray Antiperspirant

Manufacturer
Conopco Inc. d/b/a/ Unilever
Effective date
2022-12-07
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:52:18

Label at a glance#

ProductSuave
Active ingredientALUMINUM CHLOROHYDRATE
Label structure10 sections

Indications and uses

reduces underarm wetness

Dosage and administration

FOR UNDERARM USE ONLY

Label contents#

Full prescribing information#

SUAVE COCONUT KISS 48HR PROTECTION DRY SPRAY ANTIPERSPIRANT - aluminum chlorohydrate aerosol, spray

DESCRIPTION SECTION

Suave Coconut Kiss 48HR Protection Dry Spray Antiperspirant

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Aluminum Chlorohydrate (23.3%)

Purpose

OTC - PURPOSE SECTION

antiperspirant

Uses

INDICATIONS & USAGE SECTION

reduces underarm wetness

Warnings

WARNINGS SECTION

• 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.

Directions

DOSAGE & ADMINISTRATION SECTION

FOR UNDERARM USE ONLY

Inactive ingredients

INACTIVE INGREDIENT SECTION

Butane, Cyclopentasiloxane, Hydrofluorocarbon 152a, Isobutane, PPG-14 Butyl Ether, Disteardimonium Hectorite, Fragrance (Parfum), Propane, BHT, Propylene Carbonate.

Questions?

OTC - QUESTIONS SECTION

Call us at 1-800-782-8301

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Suave Coconut Kiss Dry Spray APSuave Coconut Kiss Dry Spray AP

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64942-1824-12024-01-30C16284748780-11030e365-3c38-111a-e063-dadaa90a10e2Suave Coconut Kiss 48HR Protection Dry Spray Antiperspirant

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-1824-1Suave107 g in 1 CANAEROSOL, SPRAY1072

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-1824SUAVE (COCONUT KISS 48HR PROTECTION DRY SPRAY ANTIPERSPIRANT) AEROSOL, SPRAY [CONOPCO INC. D/B/A/ UNILEVER]2Legacy NDC, 1 package rows20221208_b94147de-4f9a-c943-e053-2995a90aa69e.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
64942-182464942-1824-1

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
BUTANE6LV4FOR43RIACT
CYCLOMETHICONE 50THT5PCI0RIACT
1,1-DIFLUOROETHANE0B1U8K2ME0IACT
PPG-14 BUTYL ETHERR199TJT95TIACT
DISTEARDIMONIUM HECTORITEX687XDK09LIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
PROPYLENE CARBONATE8D08K3S51EIACT
PROPANET75W9911L6IACT
ISOBUTANEBXR49TP611IACT
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
ef42fef9-4857-0874-e053-2a95a90a4e80b94147de-4f9a-c943-e053-2995a90aa69e2022-12-07WarningsExact identifier
spl id: ef42fef9-4857-0874-e053-2a95a90a4e80
spl set id: b94147de-4f9a-c943-e053-2995a90aa69e

Reported adverse events (FAERS/openFDA)#

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