Wonder Hand Fresh Gel 62% (250ml)

Manufacturer
Dai Kyoung Pharmaceutic Co.,Ltd.
Effective date
2020-04-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:07:10

Label at a glance#

ProductWonder Hand Fresh Gel 62% (250ml)
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Alcohol

INACTIVE INGREDIENT SECTION

WATER, POLYSORBATE 20, CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE, TROLAMINE, .ALPHA.-TOCOPHEROL ACETATE, GLYCERIN, GREEN TEA LEAF, FLAVOR

OTC - PURPOSE SECTION

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE 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.

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 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.

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN2
581660ethanol 0.62 ML/ML Topical GelSCD2
581660ethanol 62 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74279-0005-12022-07-29C16284748780-1e4f33bdf-a952-d8a0-e053-dadaa90a6e4ePLUS / Dai Kyoung Pharmaceutic Co.,Ltd. - Wonder Hand Fresh Gel

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74279-0005-1Wonder Hand Fresh Gel 62% (250ml)250 mL in 1 BOTTLE, PUMPGEL2502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74279-0005WONDER HAND FRESH GEL 62% (250ML) (ALCOHOL) GEL [DAI KYOUNG PHARMACEUTIC CO.,LTD.]2Legacy NDC, 1 package rows20200421_b4122b43-f5aa-4ca9-83c3-ef88332b5056.zip

Products#

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

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74279-000574279-0005-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
a3c72514-a08f-66cb-e053-2a95a90ae3b9b4122b43-f5aa-4ca9-83c3-ef88332b50562020-04-21WarningsExact identifier
spl id: a3c72514-a08f-66cb-e053-2a95a90ae3b9
spl set id: b4122b43-f5aa-4ca9-83c3-ef88332b5056

Reported adverse events (FAERS/openFDA)#

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