FDA.reportPublic FDA data

Suave Roll on Powder Antiperspirant

Manufacturer
Suave Brands Co, LLC | KDC/One Development Corporation, Inc (Knowlton)
Effective date
2026-03-30
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:52:05

Label at a glance#

ProductSuave Roll on Powder Antiperspirant
Active ingredientALUMINUM CHLOROHYDRATE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient Aluminum Chlorohydrate

INACTIVE INGREDIENT SECTION

Inactive Ingredients Water (Aqua), PPG-11 Stearyl Ether, Steareth-2, Steareth-20, Fragrance (Parfum), Glycerin, BHT, Benzyl Alcohol, Cinnamal, Cinnamyl Alcohol, Citral, Citronellol, Geraniol, Hexyl Cinnamal, Linalool

OTC - PURPOSE SECTION

Purpose antiperspirant

INDICATIONS & USAGE SECTION

Uses

  • Reduces underarm wetness
  • 24 hour protection

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Warnings

  • 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
  • Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

WARNINGS SECTION

Warnings

  • 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
  • Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

DOSAGE & ADMINISTRATION SECTION

Directions apply to underarms only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Powder roll on deo Front labelPowder roll on deo Front labelMen Powder Roll On Antiperspirant DeodorantMen Powder Roll On Antiperspirant Deodorant

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130383711005619GTIN-13: 0383711005619
EAN-13: 0383711005619
GTIN-12: 383711005619
UPC-A: 383711005619
GTIN storage (14 digits): 00383711005619		70007593_LBL-B SV AP Rollon 2.7oz Powder_PP_SG7.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83711-146-27Suave Roll on Powder Antiperspirant80 g in 1 APPLICATORGEL804

Products#

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

DailyMed product names page 1 of 1 · 18 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83711-14683711-146-27

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
CITRONELLOLP01OUT964KIACT
WATER059QF0KO0RIACT
GERANIOLL837108USYIACT
HEXYL CINNAMATE532UJ0Y6RIIACT
PPG-11 STEARYL ETHERS4G2J0Y0LGIACT
LINALOOL, (+/-)-D81QY6I88EIACT
GLYCERINPDC6A3C0OXIACT
BHT1P9D0Z171KIACT
FRAGRANCE CLEAN ORC0600327329LCV5BTFIACT
STEARETH-20L0Q8IK9E08IACT
BENZYL ALCOHOLLKG8494WBHIACT
CITRALT7EU0O9VPPIACT
STEARETH-2V56DFE46J5IACT
CINNAMALSR60A3XG0FIACT
CINNAMYL ALCOHOLSS8YOP444FIACT
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
Suave Roll on Powder AntiperspirantROLL ON ANTIPERSPIRANT DEODORANTSuave Brands Co, LLC41d5409e-1125-9d71-e063-6294a90a9be32026-03-30WarningsExact identifier
ndc (package): 83711-146-27
ndc (product): 83711-146
ndc11 (package): 83711014627
spl id: 4e45bff6-5f66-5cb3-e063-6294a90a3cc4
spl set id: 41d5409e-1125-9d71-e063-6294a90a9be3

Reported adverse events (FAERS/openFDA)#

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