Hoo gargle (Jasmine Flavor)(Mouthwash)

Manufacturer
MIKO CO LTD
Effective date
2022-06-24
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:49:57

Label at a glance#

ProductHoo gargle (Jasmine Flavor)(Mouthwash)
Active ingredientXYLITOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

sodium fluoride

INACTIVE INGREDIENT SECTION

menthol

xylitol

Sodium acetate

Allanine
Acetic acid
Propolis
Chitosan
Green tea extract

Stevia
Cyclodextrin
Benzoic acid
Red ginsengs extract

Caramel
Grapefruit seed extract

Maple flavor

Jasmine flavor

Purified Water

OTC - PURPOSE SECTION

dental care

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE SECTION

1. Put one cup in mouth.

2. Gargle for 30 sec ~ 1 minute

3. Spit it out.

5. Rinse with water.

WARNINGS SECTION

Be careful not to swallow it, and rinse your mouth thoroughly after use.

DOSAGE & ADMINISTRATION SECTION

dental use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
81840-1022-42024-07-30C16284748780-11030e365-02ed-111a-e063-dadaa90a10e2Drug Facts
81840-1022-42024-01-30C16284748780-11030e365-02ed-111a-e063-dadaa90a10e2Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
81840-1022-1Hoo gargle (Jasmine Flavor)(Mouthwash)10 mL in 1 CUPLIQUID102
81840-1022-2Hoo gargle (Jasmine Flavor)(Mouthwash)30 in 1 PACKAGELIQUID302
81840-1022-3Hoo gargle (Jasmine Flavor)(Mouthwash)64 in 1 PACKAGELIQUID642
81840-1022-4Hoo gargle (Jasmine Flavor)(Mouthwash)8 in 1 PACKAGELIQUID82

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
81840-1022HOO GARGLE (JASMINE FLAVOR)(MOUTHWASH) (XYLITOL) LIQUID [MIKO CO LTD]2Legacy NDC, 4 package rows20220626_e22c192c-7e1c-44ae-e053-2a95a90a433a.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
81840-102281840-1022-1, 81840-1022-2, 81840-1022-3, 81840-1022-4

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
XYLITOLVCQ006KQ1EACTIB

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
e23bcbf4-b746-2b83-e053-2a95a90ad725e22c192c-7e1c-44ae-e053-2a95a90a433a2022-06-24WarningsExact identifier
spl id: e23bcbf4-b746-2b83-e053-2a95a90ad725
spl set id: e22c192c-7e1c-44ae-e053-2a95a90a433a

Reported adverse events (FAERS/openFDA)#

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