Ilsang Doctor Hand Sanitizer Gel

Manufacturer: Soleo Cosmetic Co., Ltd.
Effective date: 2020-04-24
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: legacy-cache
Hydrated at: 2026-08-01 23:34:16

Label at a glance#

ProductIlsang Doctor Hand Sanitizer Gel

Active ingredientALCOHOL

Label structure9 sections

Indications and uses

Hand sanitizer to help reduce bacteria on the skin

Dosage and administration

Spread on both hands, rub in, let dry.

Contacts and useful links#

PhoneLabel contact(800) 764-0848

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin

Warnings

WARNINGS SECTION

Flammable, keep away from fire or flame. For external use only.

When using this product Avoid contact with eyes, ears, mouth, entire body, or damaged skins.

Stop use and ask a doctor If redness or irritation develop and persist.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children If swallowed get medical help right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Spread on both hands, rub in, let dry.

Other Information

OTHER SAFETY INFORMATION

Store at room temperature 34~86ºF (1~30ºC)

Distributed by: Firson

MADE IN KOREA

Questions?

(800) 764-0848

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Carbomer, Butylene Glycol, Phenoxyethanol, Arginine, Mugwort Extract, Yeast Extract, Luffa Extract, Fragrance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

500mL NDC: 71693-800-01

500mL Label50mL NDC: 71693-800-02 50mL Label

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

Ilsang Doctor Hand Sanitizer Gel
Ethyl Alcohol
ARTEMISIA PRINCEPS LEAF
YEAST, UNSPECIFIED
LUFFA
ARGININE
ALCOHOL
WATER
CARBOMER 940
BUTYLENE GLYCOL
PHENOXYETHANOL
GLYCERIN

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
71693-800	71693-800-01, 71693-800-02

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
ARTEMISIA PRINCEPS LEAF	SY077EW02G	IACT
YEAST, UNSPECIFIED	3NY3SM6B8U	IACT
LUFFA	F0R3Y60C6V	IACT
ARGININE	94ZLA3W45F	IACT
ALCOHOL	3K9958V90M	ACTIB
WATER	059QF0KO0R	IACT
CARBOMER 940	4Q93RCW27E	IACT
BUTYLENE GLYCOL	3XUS85K0RA	IACT
PHENOXYETHANOL	HIE492ZZ3T	IACT
GLYCERIN	PDC6A3C0OX	IACT

Source Document#

Source XML · Source PDF

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
b3f73f87-8d36-ac8a-e053-2995a90a7695			a1b31c0d-ef20-56be-e053-2a95a90a7e4b	2020-11-13	Warnings	Exact identifier spl set id: a1b31c0d-ef20-56be-e053-2a95a90a7e4b

Reported adverse events (FAERS/openFDA)#

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