FDA.reportPublic FDA data

Dial Professional Gel Sanitizer

Manufacturer
Henkel Corporation
Effective date
2025-12-11
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:21:49

Label at a glance#

ProductDial Professional Gel Sanitizer
Active ingredientALCOHOL
Label structure6 sections

Label contents#

Full prescribing information#

Dial Hand Sanitzer (Gel/Foaming)

OTC - ACTIVE INGREDIENT SECTION

Dial Professional Gel Hand Sanitizer

Active Ingredient: Ethyl Alcohol 62.0% v/v Purpose: Antiseptic

Warnings

WARNINGS SECTION

Warnings For external use only
Flammable. Keep away from fire or flame.

When using this product•Avoid contact with face, eyes, and broken skin. •If eye contact occurs, flush thoroughly with water and seek medical advice.ORWhen using this productavoid contact with face, eyes, and broken skin.If eye contact occurs, flush thoroughly with water and seek medical advice.
Stop use and ask a doctor if•Irritation or redness developsORStop use and ask a doctor ifirritation or redness develops
Keep out of reach of children. •If swallowed, get medical help or contact a Poison Control Center right away

DOSAGE & ADMINISTRATION SECTION

Use(s)Hand sanitizer to help reduce bacteria thatpotentially may cause disease

INDICATIONS & USAGE SECTION

Use(s)Hand sanitizer to help reduce bacteria that potentially may cause disease

INACTIVE INGREDIENT SECTION

Inactive ingredients Aqua (Water, Eau) · Propylene Glycol ·

Glycerin . Carbomer . Aminomethyl Propanol . Isopropyl Myristate .
T-Butyl Alcohol

Dial Gel/Foaming Hand Sanitizer

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FOP and BOP 11 Fl OZFOP and BOP 11 Fl OZ

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54340-136-01Dial Professional Gel Sanitizer1200 mL in 1 BOTTLE, DISPENSINGGEL12002
54340-136-02Dial Professional Gel Sanitizer3 in 1 CARTONGEL32
54340-136-03Dial Professional Gel Sanitizer221 mL in 1 BOTTLE, PUMPGEL2212
54340-136-04Dial Professional Gel Sanitizer12 in 1 CARTONGEL122
54340-136-05Dial Professional Gel Sanitizer443 mL in 1 POUCHGEL4432
54340-136-06Dial Professional Gel Sanitizer6 in 1 CARTONGEL62
54340-136-07Dial Professional Gel Sanitizer1000 mL in 1 BOTTLE, DISPENSINGGEL10002
54340-136-08Dial Professional Gel Sanitizer3 in 1 CARTONGEL32
54340-136-09Dial Professional Gel Sanitizer59 mL in 1 BOTTLE, DISPENSINGGEL592
54340-136-10Dial Professional Gel Sanitizer144 in 1 CARTONGEL1442
54340-136-11Dial Professional Gel Sanitizer325 mL in 1 BOTTLE, PUMPGEL3252
54340-136-11Dial Professional Gel Sanitizer12 in 1 CARTONGEL122

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54340-13654340-136-01, 54340-136-02, 54340-136-03, 54340-136-04, 54340-136-05, 54340-136-06, 54340-136-07, 54340-136-08, 54340-136-09, 54340-136-10, 54340-136-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT

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 Gel SanitizerDIAL PROFESSIONAL GEL HAND SANITIZERHenkel Corporation28dadc94-e802-9fbb-e063-6394a90a79982025-12-11WarningsExact identifier
ndc (package): 54340-136-09
ndc (package): 54340-136-11
ndc (package): 54340-136-06
ndc (package): 54340-136-01
ndc (package): 54340-136-10
ndc (package): 54340-136-07
ndc (package): 54340-136-08
ndc (package): 54340-136-02
ndc (package): 54340-136-03
ndc (package): 54340-136-05
ndc (package): 54340-136-04
ndc (product): 54340-136
ndc11 (package): 54340013601
ndc11 (package): 54340013606
ndc11 (package): 54340013608
ndc11 (package): 54340013605
ndc11 (package): 54340013604
ndc11 (package): 54340013603
ndc11 (package): 54340013602
ndc11 (package): 54340013610
ndc11 (package): 54340013607
ndc11 (package): 54340013609
ndc11 (package): 54340013611
spl id: 45afb1bf-2b44-de57-e063-6394a90a9673
spl set id: 28dadc94-e802-9fbb-e063-6394a90a7998

Reported adverse events (FAERS/openFDA)#

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