COSMERIT Hand Sanitizer 1G

Manufacturer
Interkos Co.,Ltd.
Effective date
2020-07-04
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:20:06

Label at a glance#

ProductCOSMERIT Hand Sanitizer 1G
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Alcohol

INACTIVE INGREDIENT SECTION

Water, Carbomer, Triethanolamine, PEG-60 Hydrogenated Castor Oil, Fragrance, Chlorphenesin, Trideceth-10, Butylene Glycol, Origanum Vulgare Leaf Extract, Chamaecyparis Obtusa Leaf Extract, Salix Alba (Willow) Bark Extract, Cinnamomum Cassia Bark Extract, Lactobacillus/Soybean Ferment Extract, Portulaca Oleracea Extract, Vincetoxicum Atratum Extract, Scutellaria Baicalensis Root Extract, 1,2-Hexanediol, Caprylyl Glycol, Aloe Barbadensis Leaf Extract, Illicium Verum (Anise) Fruit Extract

OTC - PURPOSE SECTION

■ instant healthcare personnel hand antiseptic to reduce bacteria that potentially can cause disease

■ instant hand antiseptic to decrease bacteria on the skin

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE SECTION

Pump an appropriate amount on to the hands and rub together until dry

WARNINGS SECTION

1. Do not use this product on the following parts of body. Around eyes and ears, oral cavity, large area of the
parts of body, or wounded skins (It may cause irritations)
2. Stop using at once in case of the following symptoms, and seek medical advice. 1) When eczema, red spots,
itchiness, edema, and allergic reactions occur. 2)When skin irritations happen.
3. Other user reminders 1) For external use only(No oral intake). 2) Avoid contact with eyes, and in case contact
occurs, rinse it thoroughly with clean water and consult a doctor or pharmacist. 3) When you use it on a large skin
area or use it long-termly, please be aware that vapor is not absorbed. (If Ethanol vapor is largely and repeatedly
inhaled and absorbed, it may cause irritation to mucous membrane and headache might occur.) 4)When the product
is used on the same part of skin repeatedly, the skin may become rough due to skimming. 5) Do not use with sealed
gauze bandage, Gibbs bandage or pack, as irritations may occur. 6) Do not use this product while anus and vagina
steaming as irritations or chemical burns may occur. 7) Do not use for purposes other than specified.

DOSAGE & ADMINISTRATION SECTION

external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77049-0003-12022-01-28C16284748780-1d6a99b39-4278-a426-e053-dadaa90af4c2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
77049-0003-1COSMERIT Hand Sanitizer 1G3785 mL in 1 CONTAINERGEL37851

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77049-0003COSMERIT HAND SANITIZER 1G (ALCOHOL) GEL [INTERKOS CO.,LTD.]1Legacy NDC, 1 package rows20200704_a99a0dca-9037-4d1b-e053-2995a90aff5b.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77049-000377049-0003-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
a999f808-2e05-c9ff-e053-2995a90a8ff3a99a0dca-9037-4d1b-e053-2995a90aff5b2020-07-04WarningsExact identifier
spl id: a999f808-2e05-c9ff-e053-2995a90a8ff3
spl set id: a99a0dca-9037-4d1b-e053-2995a90aff5b

Reported adverse events (FAERS/openFDA)#

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