Joeten Hand Sanitizer

Manufacturer
Bender Consulting Ltd | Binh Tay Lico
Effective date
2020-04-21
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:11:29

Label at a glance#

ProductJoeten Hand Sanitizer
Active ingredientALCOHOL
Label structure12 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

Alcohol 80% 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. For use when soap and water are not available.

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

  • in children less than 2 months of age
  • on open skin wounds

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

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

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

000 mL / 00.0 fl oz 2700 mL label2700 mL label 2000 mL label2000 mL label 1800 mL Label1800 mL Label 1000 mL Label1000 mL Label 300 mL Label300 mL Label 100 mL Label100 mL Label 100 mL spray Label100 mL spray Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039339ethanol 80 % Topical SolutionPSN1
1039339ethanol 0.8 ML/ML Topical SolutionSCD1
1039339ethanol 80 % Topical SolutionSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
5eb9f24b-9328-475e-af0a-18021935eb6aProduct name120180220

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74918-001-00Joeten Hand Sanitizer100 mL in 1 BOTTLE, SPRAYLIQUID1001
74918-001-01Joeten Hand Sanitizer100 mL in 1 BOTTLELIQUID1001
74918-001-03Joeten Hand Sanitizer300 mL in 1 BOTTLELIQUID3001
74918-001-10Joeten Hand Sanitizer1000 mL in 1 BOTTLE, PUMPLIQUID10001
74918-001-18Joeten Hand Sanitizer1800 mL in 1 BOTTLELIQUID18001
74918-001-20Joeten Hand Sanitizer2000 mL in 1 BOTTLELIQUID20001
74918-001-27Joeten Hand Sanitizer2700 mL in 1 BOTTLELIQUID27001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74918-001JOETEN HAND SANITIZER (ALCOHOL) LIQUID [BENDER CONSULTING LTD]1Legacy NDC, 7 package rows20200515_a3d6bf52-2737-3793-e053-2a95a90a0552.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
74918-00174918-001-27, 74918-001-20, 74918-001-18, 74918-001-10, 74918-001-03, 74918-001-01, 74918-001-00

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 · 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
a3d6f77a-4191-7625-e053-2995a90a9918a3d6bf52-2737-3793-e053-2a95a90a05522020-04-21WarningsExact identifier
spl id: a3d6f77a-4191-7625-e053-2995a90a9918
spl set id: a3d6bf52-2737-3793-e053-2a95a90a0552

Reported adverse events (FAERS/openFDA)#

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