Doctor EL 28 Care Gargle

Manufacturer: Dr. EL CO., LTD. | BIOSTECH CO., LTD.
Effective date: 2020-07-02
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: legacy-cache
Hydrated at: 2026-08-01 23:23:00

Label at a glance#

ProductDoctor EL 28 Care Gargle

Active ingredientSODIUM FLUORIDE

Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Sodium Fluoride

OTC - PURPOSE SECTION

For dental care

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

INDICATIONS & USAGE SECTION

Gargle for 30-45 seconds with 10mL (about 1 capful) making sure it comes in to contact with all areas of the teeth. Spit out mouthwash.

WARNINGS SECTION

Don’t swallow.

In case of accidental ingestion, seek professional assistance.

Keep out of a reach of children.

Consult with a dentist or doctor for use with children under 6 years of age.wallowed, get medical help or contact a Poison Control Center right away

INACTIVE INGREDIENT SECTION

Water, Ethanol, Glycerin, PEG-40 Hydrogenated Castor Oil, Poloxamer 407, Sodium Citrate, Citric Acid, Xylitol, Menthol, Sodium Saccharin, Sucralose, Allantoin, Mentha Piperita Oil, Flavor, Glycyrrhiza Uralensis Extract, Angelica Gigas Extract, Salvia Officinalis Extract, Aloe Barbadensis Leaf Extract, Eucalyptus Globulus Leaf Extract, Calendula Officinalis Flower Extract, Propolis Extract

DOSAGE & ADMINISTRATION SECTION

For dental use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Products#

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

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

Doctor EL 28 Care Gargle
Sodium Fluoride, Tocopherol Acetate
XYLITOL
WATER
SODIUM FLUORIDE
FLUORIDE ION

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
72440-111	72440-111-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
XYLITOL	VCQ006KQ1E	IACT
WATER	059QF0KO0R	IACT
SODIUM FLUORIDE	8ZYQ1474W7	ACTIM

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
de261019-132e-609a-e053-2a95a90a4704			a981dd1a-17f0-34d2-e053-2a95a90a0219	2022-05-03	Warnings	Exact identifier spl set id: a981dd1a-17f0-34d2-e053-2a95a90a0219

Reported adverse events (FAERS/openFDA)#

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