GIFTEAST BAJA SALT GARGLE ORIGIN- sodium fluoride, sodium chloride mouthwash

GIFTEAST BAJA SALT GARGLE ORIGIN by

Drug Labeling and Warnings

GIFTEAST BAJA SALT GARGLE ORIGIN by is a Otc medication manufactured, distributed, or labeled by FOODPORT, DONG IL PHARMS CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient(s)

Sodium Fluoride 0.05%
Sodium Chloride 2.0%

Inactive ingredients

Water, Glycerin, Xylitol, PEG-40 Hydrogenated Castor Oil, Rubus Idaeus Fruit Extract, Fruit Mix Flavor, Sodium Benzoate, Polysorbate 20, Stevioside, Citric Acid, Grapefruit Flavor, Salvia Officinalis Leaf Extract, Eucalyptus Globulus Leaf Extract, Chamomilla Recutita Flower Extract, Aloe Barbadensis Leaf Extract, Mentha Piperita Oil, Citrus Limon Fruit Oil, Sodium Citrate, Menthol, Salicylic Acid, Glycyrrhiza Uralensis Root Extract

Purpose

Anticavity
Anticavity, acc

WARNINGS

■ Be careful not to swallow, and rinse your mouth thoroughly after use.
■ If this product causes abnormalities such as gum or mouth damage, please stop using it and consult your doctor or dentist.
■ Keep out of reach of children under the age of 6, and if a child under the age of 6 swallows a large amount, consult a doctor or dentist immediately.

KEEP OUT OF REACH OF CHILDREN

■ Keep out of reach of children under the age of 6, and if a child under the age of 6 swallows a large amount, consult a doctor or dentist immediately.

Use(s)

■ aids in the prevention of cavities.
■ helps prevent and reduce plaque (antiplague).
■ helps to remove bad breath.

Directions

■ adults and children 7 years of age and older : brush your teeth thoroughly, preferably after each meal or at least twice a day.
It is appropriate to use an amount of about 10ml
■ children 2 to 7 years : use about 6ml and supervise child's brushing and rinsing

Other Information

■ Store below 30℃(86℉)

Questions

www.gifteast.org

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

GIFTEAST BAJA SALT GARGLE ORIGIN 
sodium fluoride, sodium chloride mouthwash

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83445-010
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Sodium Fluoride (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	0.05 g  in 100 mL
Sodium Chloride (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698)	Sodium Chloride	2.0 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
Glycerin (UNII: PDC6A3C0OX)
Xylitol (UNII: VCQ006KQ1E)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83445-010-01	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	05/01/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/01/2023

Labeler - FOODPORT (695580479)

Registrant - FOODPORT (695580479)

Establishment
Name	Address	ID/FEI	Business Operations
DONG IL PHARMS CO., LTD.		557810721	manufacture(83445-010)