Hemirus Hand Clinic Gel

Manufacturer
GC US CORPORATION | WOOSIN COSMETICS CO.,LTD
Effective date
2020-03-30
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:04:25

Label at a glance#

ProductHemirus Hand Clinic Gel
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

hand sanitizer to help decrease bacteria on the skin. when water, soap & tower are not available recommended for repeated use

Dosage and administration

pump as needed into your palms and throughly spread on both hands. rub into skin until dry.

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Alcohol 62%

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • hand sanitizer to help decrease bacteria on the skin.
  • when water, soap & tower are not available
  • recommended for repeated use

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame

For external use only.

Do not apply around eyes. Do not use

OTC - DO NOT USE SECTION

in ears & mouth

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes.

In case of contact flush eyes with water

Stop use and ask a doctor if

OTC - ASK DOCTOR SECTION

redness or irritation develop and persist for more than 72 hours.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Children must be supervised in use of this product.

Directions

DOSAGE & ADMINISTRATION SECTION

  • pump as needed into your palms and throughly spread on both hands.
  • rub into skin until dry.

Other Information

OTHER SAFETY INFORMATION

  • Store at 20 o C (68 o to 77 o F).
  • may discolor fabrics.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Phenoxyethanol, Trolamine, Carbomer homopolymer type C (Allyl pentaerythritol crosslinked)
Methylparaben, Orange, Isopropyl myristate, D&C Orange No. 4

Questions?

OTC - QUESTIONS SECTION

  • side effects occur. You may report side effects to FDA at 1-800-FDA-1088.

ACCESSORIES

Instant Hand Sanitizer!

Kills 99.9% of Most Common Germs!

Net Wt. 16.91 fl oz. (500ml)

Manufactured by Woosincosmetics Inc.

33, Sudo-ro, 125beon-gil, Bucheon-si,
Gyeonggi-do, Korea 14491

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

500mL NDC: 71454-3039-1

500 mL label500 mL 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
71454-3039-12022-01-28C16284748780-1d6a99b39-ef46-a426-e053-dadaa90af4c2a21e0c0f-7b7e-1ec5-e053-2995a90ababb

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71454-3039-1Hemirus Hand Clinic Gel500 mL in 1 BOTTLE, PUMPGEL5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71454-3039HEMIRUS HAND CLINIC GEL (ALCOHOL) GEL [GC US CORPORATION]1Legacy NDC, 1 package rows20200331_a21e0c0f-7b7e-1ec5-e053-2995a90ababb.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71454-303971454-3039-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
a21da0ba-424e-21f7-e053-2a95a90ad48ca21e0c0f-7b7e-1ec5-e053-2995a90ababb2020-03-30WarningsExact identifier
spl id: a21da0ba-424e-21f7-e053-2a95a90ad48c
spl set id: a21e0c0f-7b7e-1ec5-e053-2995a90ababb

Reported adverse events (FAERS/openFDA)#

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