FDA.reportPublic FDA data

Dial Complete Antibacterial Hand

Manufacturer
MID-CONTINENT PACKAGING, INC.
Effective date
2021-04-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:40:12

Label at a glance#

ProductDial Complete Antibacterial Hand Spring Water
Active ingredientBenzalkonium Chloride
Label structure10 sections

Indications and uses

For handwashing to decrease bacteria on the skin.

Dosage and administration

Pump into hands, wet as needed Lather vigorously for at least 15 seconds Wash skin, rinse thoroughly and dry

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

  • For handwashing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or 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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Pump into hands, wet as needed
  • Lather vigorously for at least 15 seconds
  • Wash skin, rinse thoroughly and dry

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua (Water, Eau) • Lauramidopropylamine Oxide • Glycerin • Cetrimonium Chloride • Lauramine Oxide • Sodium Chloride • PEG-120 Methyl Glucose Dioleate • Citric Acid • Sodium Benzoate • Myristamidopropylamine Oxide • Parfum (Fragrance) • Zinc Sulfate • Dimethyl Lauramine • Tetrasodium EDTA • Alcohol • Dimethyl Myristamine • CI 42090 (Blue 1) • CI 17200 (Red 33)

Questions?

OTC - QUESTIONS SECTION

1-800-258-DIAL (3425)

SPL UNCLASSIFIED SECTION

Distributed by
Henkel Corporation,
Rocky Hill, CT 06067

PRINCIPAL DISPLAY PANEL - 1.53 L Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

KILLS 99.9% OF BACTERIA*

NEW
LOOK!

Dial
COMPLETE®

LIQUID
antibacterial
Hand Soap

SPRING
WATER®

52 FL OZ (1.62 QT) 1.53 L

2370134

PRINCIPAL DISPLAY PANEL - 1.53 L Bottle Label
PRINCIPAL DISPLAY PANEL - 1.53 L Bottle Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN1
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD1
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY1
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f47a510b-6679-4664-b2d6-47b5c4afe7ccProduct name420260217
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69560-234-022025-01-30C16284748780-12cef2736-655d-d83d-e063-dadaa90ab31fDial Complete ® Antibacterial Liquid Hand Soap Spring Water ®

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69560-234-02Dial Complete Antibacterial Hand Spring Water1530 mL in 1 BOTTLE, PLASTICSOLUTION15301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69560-234DIAL COMPLETE ANTIBACTERIAL HAND SPRING WATER (BENZALKONIUM CHLORIDE) SOLUTION [MID-CONTINENT PACKAGING, INC.]1Legacy NDC, 1 package rows20210506_c55888fc-c2ff-4d29-ba3e-2ad36c87832e.zip

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69560-23469560-234-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
Benzalkonium ChlorideF5UM2KM3W7ACTIB
Water059QF0KO0RIACT
Lauramidopropylamine OxideI6KX160QTVIACT
Lauramine Oxide4F6FC4MI8WIACT
Cetrimonium ChlorideUC9PE95IBPIACT
GLYCERINPDC6A3C0OXIACT
Sodium Chloride451W47IQ8XIACT
PEG-120 METHYL GLUCOSE DIOLEATEYM0K64F20VIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
Sodium BenzoateOJ245FE5EUIACT
Edetate SodiumMP1J8420LUIACT
Myristamidopropylamine Oxide3HSF539C9TIACT
Zinc Sulfate HeptahydrateN57JI2K7WPIACT
Dimethyl Lauramine6V2OM30I1ZIACT
Alcohol3K9958V90MIACT
Dimethyl Myristamine5E4O85D8T2IACT
FD&C BLUE NO. 1H3R47K3TBDIACT
D&C RED NO. 339DBA0SBB0LIACT

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
0e5de26c-4336-4e49-89c7-38a694dd43e9c55888fc-c2ff-4d29-ba3e-2ad36c87832e2021-04-26WarningsExact identifier
spl id: 0e5de26c-4336-4e49-89c7-38a694dd43e9
spl set id: c55888fc-c2ff-4d29-ba3e-2ad36c87832e

Reported adverse events (FAERS/openFDA)#

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