dial Professional Foaming Hand Sanitizer

Manufacturer
Zotos International Inc
Effective date
2020-05-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:09:22

Label at a glance#

Productdial Professional Foaming Hand Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Dosage and administration

Put foam into DRY hands, wet hands thoroughly and rub into skin until dry. Children under 6 years of age should be supervised by an adult when using this product.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 65% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease.

Warnings

WARNINGS SECTION

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.

Stop use and ask a doctor if irritation or redness develops.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Put foam into DRY hands, wet hands thoroughly and rub into skin until dry.
  • Children under 6 years of age should be supervised by an adult when using this product.

Inactive ingredients

INACTIVE INGREDIENT SECTION


Aqua (Water, Eau)· PEG-10 Dimethicone · Glycerin · Cocamidopropyl PG-Dimonium Chloride· lsopropyl Myristate ·
PEG-12 Allyl Ether· T-Butyl Alcohol · Diazolidinyl Urea · Methylparaben

Questions

OTC - QUESTIONS SECTION

1-877-777-3277

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FrontFrontbackback450 mL NDC: 50663-004-01

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50663-004-012022-01-28C16284748780-1d6a99b39-bee4-a426-e053-dadaa90af4c2Dial Professional Foaming Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50663-004-01dial Professional Foaming Hand Sanitizer450 mL in 1 BOTTLE, DISPENSINGLIQUID4501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50663-004DIAL PROFESSIONAL FOAMING HAND SANITIZER LIQUID [ZOTOS INTERNATIONAL INC]1Legacy NDC, 1 package rows20200502_a499f12b-cbe4-2169-e053-2995a90a5c8e.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50663-00450663-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Source Document#

Source XML · Source PDF

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
a499f467-26aa-7c4f-e053-2995a90aa26fa499f12b-cbe4-2169-e053-2995a90a5c8e2020-05-01WarningsExact identifier
spl id: a499f467-26aa-7c4f-e053-2995a90aa26f
spl set id: a499f12b-cbe4-2169-e053-2995a90a5c8e

Reported adverse events (FAERS/openFDA)#

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