FDA.reportPublic FDA data

Dial Professional Roll On Anti Perspirant Deodorant

Manufacturer
Henkel Corporation
Effective date
2025-12-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:22:12

Label at a glance#

ProductDial Professional Roll On Anti Perspirant Deodorant
Active ingredientALUMINUM CHLOROHYDRATE
Label structure8 sections

Indications and uses

Reduces underarm wetness

Dosage and administration

apply to underarms only

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chlorohydrate 16.0%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Uses

INDICATIONS & USAGE SECTION

Reduces underarm wetness

Warnings

WARNINGS SECTION

Warnings
For external use only
Do not use on broken skin
Stop use if rash or irritation occurs
Ask a doctor before use if you have
kidney disease.
Keep out of reach of children. If
swallowed, get medical help or contact
a Poison Control Center right away

When using this product

OTC - WHEN USING SECTION

  • avoid contact with eyes. In case of eye contact, flush with water.

Stop using and ask doctor if

OTC - STOP USE SECTION

  • irritation or redness develops

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

apply to underarms only

Inactive ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredients:
Aqua (Water, Eau) · Steareth-2 ·
Steareth-21 . Phenoxyethanol .
Parfum (Fragrance) . PPG-15
Stearyl Ether . Aluminum Starch
Octenylsuccinate

Questions?

OTC - QUESTIONS SECTION

1-877-777-3277

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

AntiPerspirant DeodorantAntiPerspirant Deodorant

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130080196736648GTIN-13: 0080196736648
EAN-13: 0080196736648
GTIN-12: 080196736648
UPC-A: 080196736648
GTIN storage (14 digits): 00080196736648		APDO-1.5FLOz_FJM23KW0003-01 .jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54340-018-01Dial Professional Roll On Anti Perspirant Deodorant44 mL in 1 BOTTLESOLUTION441
54340-018-02Dial Professional Roll On Anti Perspirant Deodorant48 in 1 CARTONSOLUTION481

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54340-01854340-018-01, 54340-018-02

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
PPG-15 STEARYL ETHER1II18XLS1LIACT
ALUMINUM STARCH OCTENYLSUCCINATEI9PJ0O6294IACT
PHENOXYETHANOLHIE492ZZ3TIACT
WATER059QF0KO0RIACT
STEARETH-2V56DFE46J5IACT
STEARETH-2153J3F32P58IACT
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
Dial Professional Roll On Anti Perspirant DeodorantALUMINUM CHLOROHYDRATE 16 PERCENTHenkel Corporation45b1a3ee-929f-f8ac-e063-6294a90a62782025-12-11WarningsExact identifier
ndc (package): 54340-018-01
ndc (package): 54340-018-02
ndc (product): 54340-018
ndc11 (package): 54340001801
ndc11 (package): 54340001802
spl id: 45b19b32-0e55-e8bd-e063-6294a90a8bb7
spl set id: 45b1a3ee-929f-f8ac-e063-6294a90a6278

Reported adverse events (FAERS/openFDA)#

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