FDA.reportPublic FDA data

Duke Cannon Prescott

Manufacturer
VVF Kansas Services LLC | VVF Kansas Services, LLC
Effective date
2022-12-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:52:47

Label at a glance#

ProductDuke Cannon Prescott
Active ingredientALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY
Label structure12 sections

Indications and uses

• Reduces underarm wetness • Extra effective

Dosage and administration

Apply to underarms only.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Zirconium Trichlorohydrex GLY 20%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Uses

INDICATIONS & USAGE SECTION

• Reduces underarm wetness

• Extra effective

Warnings:

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

Do not use on broken skin.

OTC - STOP USE SECTION

Stop use if rash or irritation occurs.

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have kidney disease.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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, Stearyl Alcohol, Polyglyceryl-3 Caprate (Beeswax),

Aluminum Starch Octenylsuccinate, Fragrance, Glycerin, Dimethicone,

Hydrogenated Castor Oil, Silica, Aloe Barbadensis (Aloe) Leaf Juice,

Hamamelis Virginiana (Witch Hazel) Distillate, Tocopheryl Acetate (Vitamin E),

Charcoal Powder

SPL UNCLASSIFIED SECTION

DIST. BY: DUKE CANNON SUPPLY CO.

MINNEAPOLIS, MN 55401

MADE IN THE USA

UPC 3-71782-00083-1

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DC Prescott AP Labels 2022DC Prescott AP Labels 2022

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10889-428-012024-01-30C16284748780-11030e365-66c8-111a-e063-dadaa90a10e2Duke Cannon Antiperspirant - Prescott

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10889-428-01Duke Cannon Prescott85 g in 1 APPLICATORSTICK851

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10889-428DUKE CANNON PRESCOTT (ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY) STICK [VVF KANSAS SERVICES LLC]1Legacy NDC, 1 package rows20221230_f0fd79fe-bf77-cc51-e053-2a95a90a363d.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10889-42810889-428-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALUMINUM STARCH OCTENYLSUCCINATEI9PJ0O6294IACT
ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLYT27D6T99LHACTIB
STEARYL ALCOHOL2KR89I4H1YIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
ACTIVATED CHARCOAL2P3VWU3H10IACT
CYCLOMETHICONE 50THT5PCI0RIACT
GLYCERINPDC6A3C0OXIACT

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
f0fd79fe-bf78-cc51-e053-2a95a90a363df0fd79fe-bf77-cc51-e053-2a95a90a363d2022-12-29WarningsExact identifier
spl id: f0fd79fe-bf78-cc51-e053-2a95a90a363d
spl set id: f0fd79fe-bf77-cc51-e053-2a95a90a363d

Reported adverse events (FAERS/openFDA)#

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