MUDSOO BACTERIA ZERO MASK MIST

Manufacturer
INTERKOS CO., LTD.
Effective date
2020-10-22
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:10:17

Label at a glance#

ProductMUDSOO BACTERIA ZERO MASK MIST
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

alcohol

INACTIVE INGREDIENT SECTION

Water
Glycerin
Mentha Arvensis Leaf Oil
Melaleuca Alternifolia (Tea Tree) Leaf Oil
Eugenia Caryophyllus (Clove) Bud Oil

OTC - PURPOSE SECTION

Providing anti-germ effects by direct injection onto the masks and pleasant use.Clove oils and Tea tree oils, natural originated vegetable oils, protect the harmfulenvironment with protecting the bad breath with peppermint oils.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE SECTION

After injecting onto disposable masks, use the masks when they are completely dried. (It isalso available on any fabric materials.)

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 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77049-000577049-0005-1

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
7d2301e3-823c-437b-8769-8fb55bb15596b248ca6e-34d6-0773-e053-2995a90ac7fb2021-11-22WarningsExact identifier
spl set id: b248ca6e-34d6-0773-e053-2995a90ac7fb

Reported adverse events (FAERS/openFDA)#

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