FDA.reportPublic FDA data

Suave

Manufacturer
Conopco Inc. d/b/a Unilever
Effective date
2022-12-07
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-05-31 23:52:07

Label at a glance#

ProductSuave Clinical Protection Coconut Kiss
Active ingredientALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Aluminum Zirconium Tetrachlorohydrex GLY (20%)

OTC - PURPOSE SECTION

Purpose
anti-perspirant

WARNINGS SECTION

Warnings
For external use only

OTC - DO NOT USE SECTION

Do not use on broken skin

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have kidney disease

OTC - STOP USE SECTION

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.

INDICATIONS & USAGE SECTION

Uses
▪  reduces underarm wetness
▪  24 hour protection
▪  extra effective

DOSAGE & ADMINISTRATION SECTION

Directions
▪  apply to underarms only
▪  before bed, apply two clicks of product to each underarm

INACTIVE INGREDIENT SECTION

Inactive ingredients  Cyclopentasiloxane, Dimethicone, Paraffin, Microcrystalline Wax, Fragrance (Parfum), Silica, Dimethicone Crosspolymer, BHT.

OTC - QUESTIONS SECTION

Questions?  Call toll-free 1-800-782-8301

1.7 oz PDP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SuaveClinicalCoconutKissPDPSuaveClinicalCoconutKissPDP

1.7 oz carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SuaveClinicalCoconutKisscartonSuaveClinicalCoconutKisscarton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64942-1438-22024-01-30C16284748780-19d75b9cf-f593-f424-e053-dadaa90a57ceSuave Clinical Protection Coconut Kiss antiperspirant deodorant
64942-1438-22020-10-30C16284748780-19d75b9cf-f593-f424-e053-dadaa90a57ceSuave Clinical Protection Coconut Kiss antiperspirant deodorant
64942-1438-22020-01-31C16284748780-19d75b9cf-f593-f424-e053-dadaa90a57ceSuave Clinical Protection Coconut Kiss antiperspirant deodorant

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-1438-1SuaveClinical Protection Coconut Kiss48 g in 1 CONTAINERSTICK485
64942-1438-2SuaveClinical Protection Coconut Kiss1 in 1 CARTONSTICK15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-1438SUAVE CLINICAL PROTECTION COCONUT KISS (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY) STICK [CONOPCO INC. D/B/A UNILEVER]5Legacy NDC, 2 package rows20221208_652fb47c-aaaf-40c6-9300-c19d118b4260.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
64942-143864942-1438-1, 64942-1438-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
CYCLOMETHICONE 50THT5PCI0RIACT
DIMETHICONE92RU3N3Y1OIACT
MICROCRYSTALLINE WAXXOF597Q3KYIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
PARAFFINI9O0E3H2ZEIACT
BUTYLATED HYDROXYTOLUENE1P9D0Z171KIACT
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY8O386558JEACTIB

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
ef3c9dbe-ddfc-9384-e053-2995a90af83e652fb47c-aaaf-40c6-9300-c19d118b42602022-12-07WarningsExact identifier
spl id: ef3c9dbe-ddfc-9384-e053-2995a90af83e
spl set id: 652fb47c-aaaf-40c6-9300-c19d118b4260

Reported adverse events (FAERS/openFDA)#

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