Raon Hand Sanitizer Gel

Manufacturer
Liz Corporation Co., Ltd
Effective date
2021-02-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:38:26

Label at a glance#

ProductRaon Hand Sanitizer Gel
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

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

Storage and handling

Store between 15-30ºC (59-86ºF) Avoid Freezing and excessive heat above 40ºC (104ºF)

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70.0%

Purpose

OTC - PURPOSE SECTION

ANTISEPTIC

Use

DOSAGE & ADMINISTRATION SECTION

Hand sanitizer to decrease bacteria on the skin that could cause disease

Warnings

WARNINGS SECTION

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

When using this product

OTC - WHEN USING SECTION

Keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest.

Stop use and ask a doctor if

OTC - STOP USE SECTION

skin irritation or rash 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

INDICATIONS & USAGE SECTION

Place enough product on hands to cover all surfaces. Rub hands together until dry

Superevise children under 6 years of age when using this product to avoid swalloing.

Other information

STORAGE AND HANDLING SECTION

Store between 15-30ºC (59-86ºF)

Avoid Freezing and excessive heat above 40ºC (104ºF)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Butylene Glycol, Carbomer, Triethanplamine, Aloe Barbadensis Leaf Extract, Artemisia Vulgaris Extract

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

79487-202-0179487-202-01

79487-202-0279487-202-02

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79487-202-012023-01-30C16284748780-1f386c649-eb51-0266-e053-dadaa90a7c1a79487-202 Raon Hand Sanitizer Gel
79487-202-022023-01-30C16284748780-1f386c649-eb51-0266-e053-dadaa90a7c1a79487-202 Raon Hand Sanitizer Gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79487-202-01Raon Hand Sanitizer Gel500 mL in 1 BOTTLE, PUMPGEL5001
79487-202-02Raon Hand Sanitizer Gel50 mL in 1 BOTTLE, PUMPGEL501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79487-202RAON HAND SANITIZER GEL (ALCOHOL) GEL [LIZ CORPORATION CO., LTD]1Legacy NDC, 2 package rows20210223_bbf7beda-307c-75e9-e053-2a95a90a9f33.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79487-20279487-202-01, 79487-202-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
bbf7beda-307d-75e9-e053-2a95a90a9f33bbf7beda-307c-75e9-e053-2a95a90a9f332021-02-22WarningsExact identifier
spl id: bbf7beda-307d-75e9-e053-2a95a90a9f33
spl set id: bbf7beda-307c-75e9-e053-2a95a90a9f33

Reported adverse events (FAERS/openFDA)#

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