MOR HAND SANITIZER

Manufacturer
ARDERIN DISTILLERY LIMITED
Effective date
2020-05-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:15:13

Label at a glance#

ProductMOR HAND SANITIZER
Active ingredientALCOHOL
Label structure9 sections

Dosage and administration

Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

ACTIVE INGREDIENT(S)

OTC - ACTIVE INGREDIENT SECTION

Ethanol 70%

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

USE[S]

INDICATIONS & USAGE SECTION

Health care personnel hand rub to help reduce bacteria that potentially can cause disease.

WARNINGS

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame.

Do not use

  • In children less than 2 months of age
  • On open skin wounds

When using this product keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water. 

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition. 

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

  • Place enough product on hands to cover all surfaces. Rub hands together until dry.
  • Supervise children under 6 years of age when using this product to avoid swallowing.

OTHER INFORMATION

STORAGE AND HANDLING SECTION

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Glycerin, Hydrogen Peroxide, Purified Water USP

SPL UNCLASSIFIED SECTION

ESTABLISHED IN TULLAMORE

Ireland

ANTISEPTIC HAND RUB

NON-STERILE SOLUTION

PRODUCED IN IRELAND

www.MorIrishGin.com

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN1
582753ethanol 0.7 ML/ML Topical SolutionSCD1
582753ethanol 70 % Topical SolutionSY1
582753ethyl alcohol 70 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78375-001-252021-07-23C16284748780-1c7ccaba7-1428-fd44-e053-dadaa90aa01bMOR HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78375-001-25MOR HAND SANITIZER250 mL in 1 BOTTLE, PLASTICSOLUTION2501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78375-001MOR HAND SANITIZER (ALCOHOL) SOLUTION [ARDERIN DISTILLERY LIMITED]1Legacy NDC, 1 package rows20200529_c6dad420-ae09-4bf2-93db-60f70e4a0caf.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
78375-00178375-001-25

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

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
f329c311-bd6b-48ed-94a0-65f90fde9a58c6dad420-ae09-4bf2-93db-60f70e4a0caf2020-05-26WarningsExact identifier
spl id: f329c311-bd6b-48ed-94a0-65f90fde9a58
spl set id: c6dad420-ae09-4bf2-93db-60f70e4a0caf

Reported adverse events (FAERS/openFDA)#

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