Hemirus Hand Clinic Gel 70%

Manufacturer: GC US CORPORATION | WOOSIN COSMETICS CO.,LTD
Effective date: 2020-03-31
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:04:35

Label at a glance#

ProductHemirus Hand Clinic Gel 70%

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.

Contacts and useful links#

PhoneFDA MedWatch1-800-FDA-1088

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70%

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 ^oC (68 ^o to 77 ^oF).
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, Denatonium benzoate

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: 71454-3041-1

500 ml label

100mL NDC: 71454-3041-2

100 ml label

30mL NDC: 71454-3041-3

30 ml label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
581662	ethanol 70 % Topical Gel	PSN	1
581662	ethanol 0.7 ML/ML Topical Gel	SCD	1
581662	ethanol 70 % Topical Gel	SY	1
581662	ethyl alcohol 70 % Topical Gel	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
71454-3041-1	2022-01-28	C162847	48780-1	d6a99b39-ef4c-a426-e053-dadaa90af4c2	a223b67c-10b1-07f8-e053-2a95a90ace3a
71454-3041-2	2022-01-28	C162847	48780-1	d6a99b39-ef4c-a426-e053-dadaa90af4c2	a223b67c-10b1-07f8-e053-2a95a90ace3a
71454-3041-3	2022-01-28	C162847	48780-1	d6a99b39-ef4c-a426-e053-dadaa90af4c2	a223b67c-10b1-07f8-e053-2a95a90ace3a

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
71454-3041-1	Hemirus Hand Clinic Gel 70%	500 mL in 1 BOTTLE, PUMP	GEL	500	1
71454-3041-2	Hemirus Hand Clinic Gel 70%	100 mL in 1 TUBE	GEL	100	1
71454-3041-3	Hemirus Hand Clinic Gel 70%	30 mL in 1 TUBE	GEL	30	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71454-3041	HEMIRUS HAND CLINIC GEL 70% (ALCOHOL) GEL [GC US CORPORATION]	1	Legacy NDC, 3 package rows	20200401_a223b67c-10b1-07f8-e053-2a95a90ace3a.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

Hemirus Hand Clinic Gel 70%
Alcohol
WATER
PHENOXYETHANOL
TROLAMINE
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED)
METHYLPARABEN
ORANGE
ISOPROPYL MYRISTATE
D&C ORANGE NO. 4
DENATONIUM BENZOATE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
71454-3041	71454-3041-1, 71454-3041-2, 71454-3041-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
WATER	059QF0KO0R	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
TROLAMINE	9O3K93S3TK	IACT
CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED)	4Q93RCW27E	IACT
METHYLPARABEN	A2I8C7HI9T	IACT
ORANGE	5EVU04N5QU	IACT
ISOPROPYL MYRISTATE	0RE8K4LNJS	IACT
D&C ORANGE NO. 4	Q1LIY3BO0U	IACT
DENATONIUM BENZOATE	4YK5Z54AT2	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
a223b67c-10b0-07f8-e053-2a95a90ace3a			a223b67c-10b1-07f8-e053-2a95a90ace3a	2020-03-31	Warnings	Exact identifier spl id: a223b67c-10b0-07f8-e053-2a95a90ace3a spl set id: a223b67c-10b1-07f8-e053-2a95a90ace3a

Reported adverse events (FAERS/openFDA)#

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