Suave

Manufacturer: Conopco Inc. d/b/a/ Unilever
Effective date: 2022-12-07
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-05-31 23:52:06

Label at a glance#

ProductSuave Powder 24 Hour Protection Roll-On AntiPerspirant Deodorant

Active ingredientALUMINUM CHLOROHYDRATE

Label structure11 sections

Indications and uses

• reduces underarm wetness • 24 hour protection

Dosage and administration

apply to underarms only

Contacts and useful links#

PhoneLabel contact1-800-782-8301

Label contents#

Full prescribing information#

SUAVE POWDER 24 HOUR PROTECTION ROLL-ON ANTIPERSPIRANT DEODORANT - aluminum chlorohydrate liquid

DESCRIPTION SECTION

Suave Powder 24 Hour Protection Roll-On AntiPerspirant Deodorant

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Aluminum Chlorohydrate (22.0%)

Purpose

OTC - PURPOSE SECTION

antiperspirant

Uses

INDICATIONS & USAGE SECTION

• reduces underarm wetness
• 24 hour protection

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

Water (Aqua), PPG-11 Stearyl Ether, Steareth-2, Steareth-20, Fragrance (Parfum), Glycerin.

Questions?

OTC - QUESTIONS SECTION

Call toll-free 1-800-782-8301

INSTRUCTIONS FOR USE SECTION

Shake well with cap on
Apply to underarms
Replace cap

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SuavePowderAPDeoLabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
64942-1560-1	2024-01-30	C162847	48780-1	9d75b9d0-f343-f424-e053-dadaa90a57ce	Suave Powder 24 Hour Protection Roll-On AntiPerspirant Deodorant
64942-1560-1	2020-10-30	C162847	48780-1	9d75b9d0-f343-f424-e053-dadaa90a57ce	Suave Powder 24 Hour Protection Roll-On AntiPerspirant Deodorant
64942-1560-1	2020-01-31	C162847	48780-1	9d75b9d0-f343-f424-e053-dadaa90a57ce	Suave Powder 24 Hour Protection Roll-On AntiPerspirant Deodorant

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
64942-1560-1	SuavePowder 24 Hour Protection Roll-On AntiPerspirant Deodorant	80 mL in 1 CONTAINER	LIQUID	80		4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
64942-1560	SUAVE POWDER 24 HOUR PROTECTION ROLL-ON ANTIPERSPIRANT DEODORANT (ALUMINUM CHLOROHYDRATE) LIQUID [CONOPCO INC. D/B/A/ UNILEVER]	4	Legacy NDC, 1 package rows	20221208_5e89ba53-8db6-17d1-e053-2a91aa0a701e.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

Suave Powder 24 Hour Protection Roll-On AntiPerspirant Deodorant
ALUMINUM CHLOROHYDRATE
WATER
PPG-11 STEARYL ETHER
STEARETH-20
GLYCERIN
STEARETH-2

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
64942-1560	64942-1560-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
PPG-11 STEARYL ETHER	S4G2J0Y0LG	IACT
ALUMINUM CHLOROHYDRATE	HPN8MZW13M	ACTIB
STEARETH-20	L0Q8IK9E08	IACT
GLYCERIN	PDC6A3C0OX	IACT
STEARETH-2	V56DFE46J5	IACT

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
ef3e1c88-4877-2299-e053-2995a90a2946			5e89ba53-8db6-17d1-e053-2a91aa0a701e	2022-12-07	Warnings	Exact identifier spl id: ef3e1c88-4877-2299-e053-2995a90a2946 spl set id: 5e89ba53-8db6-17d1-e053-2a91aa0a701e

Reported adverse events (FAERS/openFDA)#

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