Dial Complete Antibacterial Foaming Hand Wash with Lotion

Manufacturer: The Dial Corporation | The Dial Corporation, West Hazelton
Effective date: 2010-01-22
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: full-release
Hydrated at: 2026-05-31 22:23:25

Label at a glance#

ProductDial Complete Antibacterial Foaming Hand Wash with Lotion Soothing White Tea, Gentle on skin

Active ingredientTRICLOSAN

Label structure11 sections

Contacts and useful links#

PhoneLabel contact1-800-258-DIAL

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient - TRICLOSAN 0.46%

Purpose - Antibacterial

OTC - PURPOSE SECTION

Uses - For handwashing to decrease bacteria on the skin

WARNINGS SECTION

Warnings - For external use only

OTC - WHEN USING SECTION

When using this product avoid contact with eyes. In case of eye contact, flush with water.

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.

SPL UNCLASSIFIED SECTION

Directions: Pump into DRY hands. Lather vigorously for at lest 15 seconds. Rinse and dry thoroughly.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Sodium Xylenesulfonate, Dipropylene Glycol, Glycerin, Sodium PCA, Camellia Sinensis Leaf Extract (White Tea Extract), Ammonium Lauryl Sulfate, Cocamidopropyl Betaine, Polyquaternium-10, Fragrance, Disodium Phosphate, Cetyl Alcohol, , Citric Acid, Methylparaben, Propylparaben, Ext. Violet 2

OTC - QUESTIONS SECTION

Questions? 1-800-258-DIAL (3425)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DC Soothing Tea 221

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DC Soothing Tea 1470

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
1053855	triclosan 0.46 % Medicated Liquid Soap	PSN	2
1053855	triclosan 4.6 MG/ML Medicated Liquid Soap	SCD	2
1053855	triclosan 0.46 % Foaming Medicated Hand Soap	SY	2
1053855	triclosan 0.46 % Medicated Liquid Soap	SY	2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
54340-809-01	2019-10-21	C162847	48780-1	956f9ecf-c786-621f-e053-dbdaa90a74ad	Drug Facts
54340-809-02	2019-10-21	C162847	48780-1	956f9ecf-c786-621f-e053-dbdaa90a74ad	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
54340-809-01	Dial Complete Antibacterial Foaming Hand Wash with LotionSoothing White Tea, Gentle on skin	221 mL in 1 BOTTLE, PUMP	SOLUTION	221		2
54340-809-02	Dial Complete Antibacterial Foaming Hand Wash with LotionSoothing White Tea, Gentle on skin	1470 mL in 1 BOTTLE, PLASTIC	SOLUTION	1470		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
54340-809	DIAL COMPLETE ANTIBACTERIAL FOAMING HAND WASH WITH LOTION SOOTHING WHITE TEA, GENTLE ON SKIN (TRICLOSAN) SOLUTION [THE DIAL CORPORATION]	2	Legacy NDC, 2 package rows	20100128_a878cbe6-b8ce-4905-a536-6f95e90d82ee.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version	Uploaded
TRICLOSAN	ACTIVE INGREDIENT	4NM5039Y5X	2
TRICLOSAN	ACTIVE MOIETY	4NM5039Y5X	2

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

Dial Complete Antibacterial Foaming Hand Wash with Lotion Soothing White Tea, Gentle on skin
TRICLOSAN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
54340-809	54340-809-01, 54340-809-02

Ingredients#

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

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

Name, UNII, Kind table
Name	UNII	Kind
TRICLOSAN	4NM5039Y5X	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
5206165a-25dc-469c-a22e-fe76d2330463			a878cbe6-b8ce-4905-a536-6f95e90d82ee	2010-01-22	Warnings	Exact identifier spl id: 5206165a-25dc-469c-a22e-fe76d2330463 spl set id: a878cbe6-b8ce-4905-a536-6f95e90d82ee

Reported adverse events (FAERS/openFDA)#

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