FDA.reportPublic FDA data

Daeyu Hand Sanitizer Pure Gel

Manufacturer
Dae Yu Co., Ltd
Effective date
2020-07-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:21:15

Label at a glance#

ProductDaeyu Hand Sanitizer Pure Gel
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

Hand sanitizer to help reduce bacteria on the skin that could cause disease.

Dosage and administration

Place enough product in your palm to thoroughly cover your hands Rub hands together briskly until dry Children under 6 years of age should be supervised when using this product

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethanol 62%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

DOSAGE & ADMINISTRATION SECTION

Hand sanitizer to help reduce bacteria on the skin that could cause disease.

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.

For external use only.

When using this product

OTC - WHEN USING SECTION

do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

Stop use and ask a doctor

OTC - ASK DOCTOR SECTION

if irritation or rash appears and lasts.

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 in your palm to thoroughly cover your hands
  • Rub hands together briskly until dry
  • Children under 6 years of age should be supervised when using this product

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Carbomer, Triethanolamine

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

500ml NDC: 79548-201-01 Label500ml NDC: 79548-201-01 Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN1
581660ethanol 0.62 ML/ML Topical GelSCD1
581660ethanol 62 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79548-201-012021-07-23C16284748780-1c7ccaba7-1bdb-fd44-e053-dadaa90aa01b79548-201

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79548-201-01Daeyu Hand Sanitizer Pure Gel500 mL in 1 BOTTLE, PUMPGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79548-201DAEYU HAND SANITIZER PURE GEL (ALCOHOL) GEL [DAE YU CO., LTD]1Legacy NDC, 1 package rows20200714_aa60883a-6b7b-ab0f-e053-2a95a90ae7f0.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79548-20179548-201-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT
WATER059QF0KO0RIACT
TROLAMINE9O3K93S3TKIACT
ALCOHOL3K9958V90MACTIB

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
aa60883a-6b7c-ab0f-e053-2a95a90ae7f0aa60883a-6b7b-ab0f-e053-2a95a90ae7f02020-07-14WarningsExact identifier
spl id: aa60883a-6b7c-ab0f-e053-2a95a90ae7f0
spl set id: aa60883a-6b7b-ab0f-e053-2a95a90ae7f0

Reported adverse events (FAERS/openFDA)#

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