Dial Professional Antibacterial Hand Sanitizer

Manufacturer: The Dial Corporation | Deb Worldwide Healthcare Inc.
Effective date: 2011-03-16
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-05-31 22:27:28

Label at a glance#

ProductDial Professional Antibacterial Hand Sanitizer

Active ingredientAlcohol

Label structure8 sections

Contacts and useful links#

PhoneLabel contact1-877-777-3277

Websitewww.dialprofessional.com

www.dialprofessional.com

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Ethyl Alcohol 72%

OTC - PURPOSE SECTION

Purpose

Antibacterial

INDICATIONS & USAGE SECTION

Uses

hand sanitizer to help reduce bacteria that potentially may cause disease

WARNINGS SECTION

Warnings

For external use only

Flammable. Keep away from fire or flame.

OTC - WHEN USING SECTION

When using this product

avoid contact with face, eyes, and broken skin. If eye contact occurs, flush thoroughly with water and seek medical advice.

OTC - STOP USE SECTION

Stop use and ask a doctor if

irritation and redness develops

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.

DOSAGE & ADMINISTRATION SECTION

Directions

pump foam into dry hands, wet thoroughly and rub into skin until dry

Children under 6 years of age should be supervised by an adult when using this product.

INACTIVE INGREDIENT SECTION

Inactive ingredients

water, n-propanol, bis-PEG-12 dimethicone, behentrimonium chloride, PEG-200 hydrogenated glyceryl palmate, PEG-7 glyceryl cocoate, coco-glucoside, glyceryl linoleammonium chloride

OTC - QUESTIONS SECTION

Questions?

1-877-777-3277

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Dial Professional

Antibacterial Hand Sanitizer Fragrance Free Foam

Kills 99.99% of germs instantly

Made in Canada

2010 Distributed by The Dial Corporation/A Henkel Company

Scottsdale, AZ 85255

www.dialprofessional.com

Install with label toward wall

Instalar con etiqueta hacia la pared

US Patent Numbers

5445288, 6082586, patent pending

1 Liter (33.8 Fl Oz)

1 QT 1.8 Fl Oz

Latex and Non-latex compatible

Tested on latex and nitrile gloves.

container label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
54340-107-12	2019-10-29	C162847	48780-1	960f7f55-bf81-8e05-e053-dbdaa90a074a	Drug Facts
54340-107-27	2019-10-29	C162847	48780-1	960f7f55-bf81-8e05-e053-dbdaa90a074a	Drug Facts

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
Alcohol	ACTIVE INGREDIENT	3K9958V90M	3
Alcohol	ACTIVE MOIETY	3K9958V90M	3
BEHENTRIMONIUM CHLORIDE	INACTIVE INGREDIENT	X7GNG3S47T	3
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE	INACTIVE INGREDIENT	0Y0NQR2GH1	3
PROPYL ALCOHOL	INACTIVE INGREDIENT	96F264O9SV	3
WATER	INACTIVE INGREDIENT	059QF0KO0R	3

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

Dial Professional Antibacterial Hand Sanitizer
Ethyl Alcohol
Alcohol
WATER
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE
PROPYL ALCOHOL
BEHENTRIMONIUM CHLORIDE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
54340-107	54340-107-27, 54340-107-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
Alcohol	3K9958V90M	ACTIB
WATER	059QF0KO0R	IACT
DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE	0Y0NQR2GH1	IACT
PROPYL ALCOHOL	96F264O9SV	IACT
BEHENTRIMONIUM CHLORIDE	X7GNG3S47T	IACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 3 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Match
PROPYL ALCOHOL	PROPYL ALCOHOL	96F264O9SV	POWDER / TOPICAL	0.4 mg/mg	Exact identifier — unii candidate 3 equally ranked IID candidates
PROPYL ALCOHOL	PROPYL ALCOHOL	96F264O9SV	OINTMENT / TOPICAL	10 %w/w	Exact identifier — unii candidate 3 equally ranked IID candidates
PROPYL ALCOHOL	PROPYL ALCOHOL	96F264O9SV	SOLUTION / TOPICAL	NA	Exact identifier — unii candidate 3 equally ranked IID candidates

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
cbcd58a3-60bb-4d12-9da3-83cb2e150982			3bbe5c32-c2b5-43ac-9918-1e6f68594bb9	2011-03-16	Warnings	Exact identifier spl id: cbcd58a3-60bb-4d12-9da3-83cb2e150982 spl set id: 3bbe5c32-c2b5-43ac-9918-1e6f68594bb9

Reported adverse events (FAERS/openFDA)#

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