Dial Spring Water Antibacterial Soap

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 22:23:27

Label at a glance#

ProductDial Spring Water Antibacterial Soap with Moisturizer
Active ingredientTRICLOSAN
Label structure12 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient - TRICLOSAN 0.15%

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 hands, wet as needed.  Lather vigorously for at lest 15 seconds. Wash skin, rinse thoroughly and dry.

INACTIVE INGREDIENT SECTION


Inactive Ingredients:  Water, Sodium Laureth Sulfate, Decyl Glucoside, Cocamidopropyl Betaine, Sodium Chloride, Cocamide MEA, Fragrance, PEG-120 Methyl Glucose Dioleate, PEG-18, Glyceryl Oleate/Cocate Aloe-Barbadensis Leaf Juice, Polyquaternium-7, DMDM Hydantoin, Tetrasodium EDTA, Citric Acid, Blue1, Red 33

OTC - QUESTIONS SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SW 221SW 221

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SW 1470SW 1470

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SW 2360SW 2360

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1020118triclosan 0.15 % Medicated Liquid SoapPSN2
1020118triclosan 1.5 MG/ML Medicated Liquid SoapSCD2
1020118triclosan 0.15 % Medicated Liquid SoapSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
54340-799-012019-10-21C16284748780-1956f9ecf-d97d-621f-e053-dbdaa90a74adDrug Facts
54340-799-022019-10-21C16284748780-1956f9ecf-d97d-621f-e053-dbdaa90a74adDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
54340-799-01Dial Spring Water Antibacterial Soapwith Moisturizer221 mL in 1 BOTTLE, PUMPSOLUTION2212
54340-799-02Dial Spring Water Antibacterial Soapwith Moisturizer591 mL in 1 BOTTLE, PLASTICSOLUTION5912

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
54340-799DIAL SPRING WATER ANTIBACTERIAL SOAP WITH MOISTURIZER (TRICLOSAN) SOLUTION [THE DIAL CORPORATION]2Legacy NDC, 2 package rows20100130_c8980c1d-9110-4b83-bf2f-2fbd946b044a.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
TRICLOSANACTIVE INGREDIENT4NM5039Y5X2
TRICLOSANACTIVE MOIETY4NM5039Y5X2

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54340-79954340-799-01, 54340-799-02

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
NameUNIIKind
TRICLOSAN4NM5039Y5XACTIB

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
d2ab64c6-776c-4019-b07d-49da210b8742c8980c1d-9110-4b83-bf2f-2fbd946b044a2010-01-22WarningsExact identifier
spl id: d2ab64c6-776c-4019-b07d-49da210b8742
spl set id: c8980c1d-9110-4b83-bf2f-2fbd946b044a

Reported adverse events (FAERS/openFDA)#

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