Duble X Concentration Gargle Liquid by DONG IL PHARMS CO.,LTD / DONG IL PHARMS CO., LTD.

Duble X Concentration Gargle Liquid by

Drug Labeling and Warnings

Duble X Concentration Gargle Liquid by is a Otc medication manufactured, distributed, or labeled by DONG IL PHARMS CO.,LTD, DONG IL PHARMS CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DUBLE X CONCENTRATION GARGLE LIQUID- cetylpyridinium chloride paste 
DONG IL PHARMS CO.,LTD

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Cetylpyridinium Chloride

Mouth is clear and cool

Plaque removal

Oral cleanliness

Oral bad breath removal

Keep out of reach of children

Three times a day, add 5 drops of this solution to the enclosed cup, add water to the marked line, gargle for about 30 seconds, and spit it out.

• Do not store above 30 ℃.
• Avoid exposure to heat, sparks and sparks.
• Be careful as it may irritate the eyes.
• In case of contact with eyes, rinse with water.
• Keep out of reach of babies and young children.

Water, Sorbitol, Flavor, Propolis Wax, Gardenia Blue Color, Chitosan, Citrus Grandis (Grapefruit) Seed Extract, Xylitol, Curcuma , Xanthorrhiza Root Extract, Stevioside, Taraxacum Platycarpum Extract, Camellia Sinensis Leaf Extract

For dental use only

DUBLE X CONCENTRATION GARGLE LIQUID 
cetylpyridinium chloride paste

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73242-0101
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P) (CETYLPYRIDINIUM - UNII:CUB7JI0JV3)	CETYLPYRIDINIUM CHLORIDE	0.0023 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
XYLITOL (UNII: VCQ006KQ1E)

Product Characteristics
Color	blue	Score
Shape		Size
Flavor	PEPPERMINT	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73242-0101-1	50 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	12/10/2019	01/02/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		12/10/2019	01/02/2020

Labeler - DONG IL PHARMS CO.,LTD (557810721)

Registrant - DONG IL PHARMS CO.,LTD (557810721)

Establishment
Name	Address	ID/FEI	Business Operations
DONG IL PHARMS CO., LTD.		557810721	manufacture(73242-0101)

Revised: 1/2020

Document Id: 9b33d775-fbf0-8347-e053-2995a90a1e8f

34390-5

Set id: 9966eade-3f2f-a7ae-e053-2995a90a2785

Version: 3

Effective Time: 20200102