Dial Complete Advanced Moisture Spring Water

Manufacturer
Zotos International Inc
Effective date
2020-11-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:33:17

Label at a glance#

ProductDial Complete Advanced Moisture Spring Water
Active ingredientBENZALKONIUM CHLORIDE
Label structure16 sections

Indications and uses

For Handwashing to decreases bacteria on the skin.

Dosage and administration

Pump into DRY hands. Later vigorously for at least 20 seconds. Rinse and dry thoroughly.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

OTC - PURPOSE SECTION

For Handwashing to decreases 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.

Stop use and ask doctor if

OTC - STOP USE SECTION

Irritation or redness develops

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed get medical help or contact a Poison Control Center right away.

Directions

INSTRUCTIONS FOR USE SECTION

Pump into DRY hands.

Later vigorously for at least 20 seconds.

Rinse and dry thoroughly.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Advanced Moisture Spring Water FHW

Aqua (Water, Eau) · Lauramidopropylamine Oxide · Cetrimonium Chloride · Glycerin · Lauramine Oxide · Citric Acid · Cocamidopropyl Betaine · Trideceth-9 · Sodium Benzoate · Myristamidopropylamine Oxide · PEG-5 Isononanoate · Parfum (Fragrance) · Zinc Sulfate · Sodium Chloride · Dimethyl Lauramine · Tetrasodium EDTA · Alcohol · Dimethyl Myristamine · CI 42090 (Blue 1) · CI 17200 (Red 33)

*Encountered in household settings

SPL UNCLASSIFIED SECTION

REFILL ONLY WITH DIAL COMPLETE FOAMING HAND WASH

INDICATIONS & USAGE SECTION

For handwashing to decrease bacteria on the skin.

Topical Liquid Solution

DOSAGE & ADMINISTRATION SECTION

Foaming Hand wash

4 Pack

SPL UNCLASSIFIED SECTION

10 FL OZ (296mL) EACH

TOTAL 40 FL OZ (1.18 L)

Artwork

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

RefillRefillInner StickerInner Stickerpage 1page 1page 2page 2page 3page 3

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN2
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD2
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY2
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50663-342-012022-01-28C16284748780-1d6a99b39-4b06-a426-e053-dadaa90af4c2Dial Complete Advanced Moisture -FHW
50663-342-022022-01-28C16284748780-1d6a99b39-4b06-a426-e053-dadaa90af4c2Dial Complete Advanced Moisture -FHW

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50663-342-01Dial Complete Advanced Moisture Spring Water1180 mL in 1 BOTTLE, PUMPSOLUTION11802
50663-342-02Dial Complete Advanced Moisture Spring Water3780 mL in 1 BOTTLE, DISPENSINGSOLUTION37802

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50663-342DIAL COMPLETE ADVANCED MOISTURE SPRING WATER (DIAL COMPLETE ADVANCED MOISTURE SPRING WATER FHW) SOLUTION [ZOTOS INTERNATIONAL INC]2Legacy NDC, 2 package rows20201110_af4a3992-6d32-db3d-e053-2995a90abafa.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50663-34250663-342-01, 50663-342-02

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
WATER059QF0KO0RIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
b3b08989-4b1c-bba1-e053-2a95a90a4af9af4a3992-6d32-db3d-e053-2995a90abafa2020-11-09WarningsExact identifier
spl id: b3b08989-4b1c-bba1-e053-2a95a90a4af9
spl set id: af4a3992-6d32-db3d-e053-2995a90abafa

Reported adverse events (FAERS/openFDA)#

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