Suave Powder

Manufacturer: Conopco Inc. d/b/a Unilever
Effective date: 2010-03-25
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 22:23:58

Label at a glance#

ProductSuave Powder Antiperspirant and Deodorant

Active ingredientAluminum Zirconium Tetrachlorohydrex GLY

Label structure9 sections

Contacts and useful links#

PhoneLabel contact1-800-782-8301

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient Purpose

Aluminum Zirconium Tetrachlorohydrex GLY(18.5%)............anti-perspirant

WARNINGS SECTION

Warning
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.

INACTIVE INGREDIENT SECTION

Inactive ingredients

Cyclopentasiloxane, dimethicone, C18-36 acid triglyceride, microcrystalline wax, silica, fragrance (parfum), dimethicone crosspolymer, BHT.

OTC - QUESTIONS SECTION

Questions? call 1-800-782-8301

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDP 2.7 oz

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
64942-0747-1	2020-01-31	C162847	48780-1	9d75b9d0-5707-f424-e053-dadaa90a57ce	Suave Powder Antiperspirant and Deodorant PDP and drug facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
64942-0747-1	Suave PowderAntiperspirant and Deodorant	76 g in 1 CONTAINER	STICK	76		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
64942-0747	SUAVE POWDER ANTIPERSPIRANT AND DEODORANT (ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY) STICK [CONOPCO INC. D/B/A UNILEVER]	1	Legacy NDC, 1 package rows	20100326_f6ab6ff0-457f-406f-928b-e0a4806d306b.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version	Uploaded
Aluminum Zirconium Tetrachlorohydrex GLY	ACTIVE INGREDIENT	8O386558JE	1
Aluminum cation	ACTIVE MOIETY	3XHB1D032B	1

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

Suave Powder Antiperspirant and Deodorant
Aluminum Zirconium Tetrachlorohydrex GLY
Aluminum cation

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
64942-0747	64942-0747-1

Ingredients#

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

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

Name, UNII, Kind table
Name	UNII	Kind
Aluminum Zirconium Tetrachlorohydrex GLY	8O386558JE	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
cec9104e-7abe-40ba-80dc-f00f90da1cbd			f6ab6ff0-457f-406f-928b-e0a4806d306b	2010-03-25	Warnings	Exact identifier spl id: cec9104e-7abe-40ba-80dc-f00f90da1cbd spl set id: f6ab6ff0-457f-406f-928b-e0a4806d306b

Reported adverse events (FAERS/openFDA)#

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