LUTHIONE HAND

Manufacturer
MYUNG COSMETIC
Effective date
2020-05-19
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 23:29:59

Label at a glance#

ProductLUTHIONE HAND
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Alcohol

INACTIVE INGREDIENT SECTION

Water, Polysorbate 20, Aminomethyl Propanol, Tocopheryl Acetate, Sodium Hyaluronate, Glycerin, Carbomer

OTC - PURPOSE SECTION

Antiseptic

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE SECTION

For the external use only

WARNINGS SECTION

Do not use on the following body parts.
Around the eyes and ears, in the oral cavity, a wide range of body parts and damaged skin (may have irritating effects)
If the following symptoms appear, stop using them immediately and consult a doctor or pharmacist.

Symptoms of skin irritation

Other precautions

For external use only
Be careful not to get into your eyes, and if so, rinse well with clean water and consult a doctor or pharmacist.
Be careful not to inhale vapor when using it extensively or for a long time. (If you drink ethanol vapor in large quantities or repeatedly, irritation to the mucous membrane, headache, etc. may occur).
When repeated use on the same site, be careful as the skin may become rough due to degreasing.
When used in sealed bandages, cast bandages, packs, etc., irritation symptoms may appear.
Do not use for any other purpose.

DOSAGE & ADMINISTRATION SECTION

Put enough amount on your hand and briskly rub hands together until it dries.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74777-03074777-030-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
POLYSORBATE 207T1F30V5YHIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
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
a5fa720e-5445-5955-e053-2a95a90ac28aa3ec6d15-67cb-2a32-e053-2a95a90aca552020-05-19WarningsExact identifier
spl id: a5fa720e-5445-5955-e053-2a95a90ac28a
spl set id: a3ec6d15-67cb-2a32-e053-2a95a90aca55

Reported adverse events (FAERS/openFDA)#

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