Soom Mouthwash

Manufacturer: BD TECHNOLOGY CO., LTD | BD TECHNOLOGY CO., LTD.
Effective date: 2020-06-10
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:17:09

Label at a glance#

ProductSoom Mouthwash

Active ingredientSODIUM FLUORIDE

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

sodium fluoride

INACTIVE INGREDIENT SECTION

Water
Sodium Fluoride
Allantoin
Erythritol
xylitol
Sodium benzoate
Glycerin
Propylene Glycol
PEG-40 Hydrogenated Castor Oil
L-Menthol
zinc gluconate
sodium citrate
Fragrance

OTC - PURPOSE SECTION

prevention of gingvitis, periodontitis, cavity, periodontal disease gum disease

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE SECTION

spit out the appropriate amount (120~15ml) for about 30 seconds after mouthing, and then brush the tooth bybrushing

WARNINGS SECTION

For oral use only.

When using this product keep out of eyes. If contact with eyes occurs, rinse promptly and thoroughly with water.

Stop use and ask a doctor if significant irritation or sensitization develops.

DOSAGE & ADMINISTRATION SECTION

for oral use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
73927-0005-1	2022-01-28	C162847	48780-1	d6a99b39-7397-a426-e053-dadaa90af4c2	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73927-0005-1	Soom Mouthwash	11 mL in 1 POUCH	LIQUID	11		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73927-0005	SOOM MOUTHWASH (SODIUM FLUORIDE) LIQUID [BD TECHNOLOGY CO., LTD]	1	Legacy NDC, 1 package rows	20200611_a7b8a58d-13fd-896e-e053-2995a90a5ec9.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

Soom Mouthwash
sodium fluoride
GLYCERIN
ALLANTOIN
WATER
FLUORIDE ION
ERYTHRITOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
73927-0005	73927-0005-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
GLYCERIN	PDC6A3C0OX	IACT
ALLANTOIN	344S277G0Z	IACT
WATER	059QF0KO0R	IACT
SODIUM FLUORIDE	8ZYQ1474W7	ACTIB
ERYTHRITOL	RA96B954X6	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
a7b8cca4-7b78-6efc-e053-2a95a90a5841			a7b8a58d-13fd-896e-e053-2995a90a5ec9	2020-06-10	Warnings	Exact identifier spl id: a7b8cca4-7b78-6efc-e053-2a95a90a5841 spl set id: a7b8a58d-13fd-896e-e053-2995a90a5ec9

Reported adverse events (FAERS/openFDA)#

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