Suave

Manufacturer
Conopco Inc. d/b/a/ Unilever
Effective date
2020-11-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:33:13

Label at a glance#

ProductSuave
Active ingredientALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
Label structure10 sections

Indications and uses

reduces underarm wetness

Dosage and administration

apply to underarms only

Label contents#

Full prescribing information#

SUAVE EXTRA FRESH 48H ANTIPERSPIRANT - aluminum zirconium tetrachlorohydrex gly stick

DESCRIPTION SECTION

Suave Extra Fresh 48H Antiperspirant

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Aluminum Zirconium Tetrachlorohydrex GLY (18.2 %)

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 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.

Directions

DOSAGE & ADMINISTRATION SECTION

apply to underarms only

Inactive ingredients

INACTIVE INGREDIENT SECTION

Cyclopentasiloxane, Isopropyl Palmitate, Stearyl Alcohol, Mineral Oil, Talc, Hydrogenated Castor Oil, Fragrance (Parfum), Steareth-100, BHT.

Questions?

OTC - QUESTIONS SECTION

Call toll-free 1-800-782-8301

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SuaveExtraFresh48HAPSuaveExtraFresh48HAP

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-1615-1Suave76 g in 1 CONTAINERSTICK762
64942-1615-2Suave2 in 1 PACKAGESTICK22

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-1615SUAVE (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY) STICK [CONOPCO INC. D/B/A/ UNILEVER]2Legacy NDC, 2 package rows20201109_785c36ab-5238-69a6-e053-2991aa0a080f.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
64942-161564942-1615-1, 64942-1615-2

Ingredients#

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

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

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
b3a0c3d2-da42-876f-e053-2a95a90abd87785c36ab-5238-69a6-e053-2991aa0a080f2020-11-08WarningsExact identifier
spl id: b3a0c3d2-da42-876f-e053-2a95a90abd87
spl set id: 785c36ab-5238-69a6-e053-2991aa0a080f

Reported adverse events (FAERS/openFDA)#

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