DUBLE X CONCENTRATION GARGLE LIQUID- cetylpyridinium chloride paste

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]

ACTIVE INGREDIENT

Cetylpyridinium Chloride

PURPOSE

Mouth is clear and cool

Plaque removal

Oral cleanliness

Oral bad breath removal

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children

INDICATIONS & USAGE

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.

WARNINGS

• 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.

INACTIVE INGREDIENT

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

DOSAGE & ADMINISTRATION

For dental use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DUBLE X CONCENTRATION GARGLE LIQUID 
cetylpyridinium chloride paste

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73242-0102
Route of Administration	DENTAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P) (CETYLPYRIDINIUM - UNII:CUB7JI0JV3)	CETYLPYRIDINIUM CHLORIDE	2.296 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: 73242-0102-1	50 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	12/10/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part356	12/10/2019

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(73242-0102)