MUDSOO BACTERIA ZERO HANDCREAM

Manufacturer
INTERKOS CO., LTD.
Effective date
2020-10-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:10:18

Label at a glance#

ProductMUDSOO BACTERIA ZERO HANDCREAM
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride

INACTIVE INGREDIENT SECTION

Water
Glycerin
Sodium Polyacrylate
Styrene/VP Copolymer
Butylene Glycol
Triethyl Citrate
PEG-60 Hydrogenated Castor Oil
1,2-Hexanediol
Caprylyl Glycol
Cetyl Ethylhexanoate
Salvia Officinalis (Sage) Oil
Trideceth-10
PEG-14M
Illicium Verum (Anise) Fruit Extract
Salix Alba (Willow) Bark Extract
Chamaecyparis Obtusa Leaf Extract
Origanum Vulgare Leaf Extract
Lactobacillus/Soybean Ferment Extract
Scutellaria Baicalensis Root Extract
Portulaca Oleracea Extract
Cinnamomum Cassia Bark Extract
Aloe Barbadensis Leaf Extract

OTC - PURPOSE SECTION

Protecting hands from the harmful environment and keeping hands healthy and clean with anti-germ effects, providing moist hands by nutrition and moisturizing.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE SECTION

1. In case of having side effects such as red rash,
swollenness or itching while using this cosmetic, or in case
such symptoms appear by direct snulight after using it,
consult a dermatologist immediately.
2. Do not apply on skin where there is wound, eczema, or irritation.
3. Storage and cautions for handling.
A. keep out of reach of children.
B. keep away from direct sunlight.

WARNINGS SECTION

1. Do not use for other purposes than its usage.2. keep away from direct sunlight or heat.3. Do not direct to people or food. .4. Do not forcibly open the cap combined to the container.5. When the content is frozen, use it on an ordinary temperature for preventing change inquality. .6. If eyes or skins are exposed to the contents, washing the area with the running waterand when the abnormal symptoms occur, consult doctors.7. Be careful when the containers are brought down and the contents may flow out.8. Directing on the higher area than eyes, the contents may be exposed to eyes and applythe contents on the sponges or the fabrics.9. Ventilation is required in sealed areas.10. When discoloring and bleaching happen on some areas for applying, please check theirpossibility in advance.11. After using the products, do not change the containers.12. If the contents are swallowed, take emergency process and consult with doctors.13. keep out of reach of children.

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77049-000777049-0007-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
c9f72b4a-1c6d-4b49-a7ad-b16e077fc5cdb2509115-562e-7456-e053-2995a90a998c2021-11-22WarningsExact identifier
spl set id: b2509115-562e-7456-e053-2995a90a998c

Reported adverse events (FAERS/openFDA)#

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