Suave Pacific Breeze

Manufacturer
Conopco Inc. d/b/a Unilever | Unilever Raeford HPCNA
Effective date
2010-05-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:24:25

Label at a glance#

ProductSuave Pacific Breeze Antiperspirant and Deodorant
Active ingredientAluminum Chlorohydrate
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient                                                                                     Purpose

Aluminum Chlorohydrate (20%).......................................antiperspirant

WARNINGS SECTION

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

OTC - QUESTIONS SECTION

Questions?
Call 1-800-782-8301

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PDP 2.6 oz
Suave Pacific Breeze 2.6 oz. PDP
Suave Pacific Breeze 2.6 oz. PDP

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64942-0891-12020-01-31C16284748780-19d75b9cf-cd58-f424-e053-dadaa90a57cePDP and Drug facts box text for Suave Pacific Breeze Antiperspirant and Deodorant

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64942-0891-1Suave Pacific BreezeAntiperspirant and Deodorant74 g in 1 CONTAINERSTICK741

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64942-0891SUAVE PACIFIC BREEZE ANTIPERSPIRANT AND DEODORANT (ALUMINUM CHLOROHYDRATE) STICK [CONOPCO INC. D/B/A UNILEVER]1Legacy NDC, 1 package rows20100506_5cdc9729-0cce-4891-9e5b-1808d967a37b.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Aluminum ChlorohydrateACTIVE INGREDIENTHPN8MZW13M1
Aluminum cationACTIVE MOIETY3XHB1D032B1

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
64942-089164942-0891-1

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
NameUNIIKind
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
58bc974e-08c1-412c-ab3e-e527ef0fe9a95cdc9729-0cce-4891-9e5b-1808d967a37b2010-05-04WarningsExact identifier
spl id: 58bc974e-08c1-412c-ab3e-e527ef0fe9a9
spl set id: 5cdc9729-0cce-4891-9e5b-1808d967a37b

Reported adverse events (FAERS/openFDA)#

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