Soom Green Mouthwash

Manufacturer
TECOZYME INC | BD TECH CO LTD
Effective date
2021-08-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:41:58

Label at a glance#

ProductSoom Green Mouthwash
Active ingredientSODIUM FLUORIDE
Label structure10 sections

Indications and uses

■ Help teeth whitening and reduce of bad breath ■ Aids in the prevention of gingivitis, periodontitis

Dosage and administration

Adults and children 6 years of age and older ■ Vigorously swish 11 mL between teeth twice a day for 30 seconds then spit out. ■ Do not swallow ■ Children under 6 years of age: do not use

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Sodium Fluoride 0.02%

PURPOSE

OTC - PURPOSE SECTION

Anticavity

Uses

INDICATIONS & USAGE SECTION

■ Help teeth whitening and reduce of bad breath
■ Aids in the prevention of gingivitis, periodontitis

WARNINGS

WARNINGS SECTION

Do not use in Children under 6 years of age
If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Do not use in Children under 6 years of age
If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 6 years of age and older
■ Vigorously swish 11 mL between teeth twice a day for 30 seconds then spit out.
■ Do not swallow
■ Children under 6 years of age: do not use

Other Information

OTHER SAFETY INFORMATION

■ Read the directions and warnings before use
■ Store at room temperature
■ This rinse is not intended to replace brushing or flossing

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Water, Erythritol, Xylitol, Sodium Benzoate, Glycerin, Allantoin, Propylene Glycol, PEG-40 Hydrogenated Caster Oil, L-Menthol, Zinc Gluconate, Sodium Citrate, Fragrance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
313029sodium fluoride 0.02 % (fluoride ion 0.01 % ) Oral RinsePSN1
313029sodium fluoride 0.2 MG/ML MouthwashSCD1
313029sodium fluoride 0.02 % (fluoride ion 0.009 % ) Oral RinseSY1
313029sodium fluoride 0.02 % (fluoride ion 0.01 % ) Oral RinseSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79717-0010-22023-01-30C16284748780-1f386c649-cf70-0266-e053-dadaa90a7c1ae1d973c2-ef96-4da5-abd2-6f4a30224850

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79717-0010-1Soom Green Mouthwash11 mL in 1 POUCHLIQUID111
79717-0010-2Soom Green Mouthwash20 in 1 CARTONLIQUID201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79717-0010SOOM GREEN MOUTHWASH (SODIUM FLUORIDE) LIQUID [TECOZYME INC]1Legacy NDC, 2 package rows20210818_e1d973c2-ef96-4da5-abd2-6f4a30224850.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79717-001079717-0010-1, 79717-0010-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
a4653787-ec8b-4a73-a52a-c978cb318420e1d973c2-ef96-4da5-abd2-6f4a302248502021-08-17WarningsExact identifier
spl id: a4653787-ec8b-4a73-a52a-c978cb318420
spl set id: e1d973c2-ef96-4da5-abd2-6f4a30224850

Reported adverse events (FAERS/openFDA)#

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