BLINGDAY BUBBLE CANDY SOLID MOUTHWASH- sodium fluoride pellet

Blingday Bubble Candy Solid Mouthwash by

Drug Labeling and Warnings

Blingday Bubble Candy Solid Mouthwash by is a Otc medication manufactured, distributed, or labeled by DongSung Pharm Co., Ltd., Dong Sung World Wide USA, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Sodium Fluoride 0.13% (0.06% w/w fluoride ion)

Drug Facts

Anticavity

Uses

Aids in the prevention of dental cavities. Helps to refresh your breath.

Warnings

Stop use and ask a dentist if oral irritation or tooth sensitivity occurs.

Warnings

Keep this out of reach of children under 6 years of age. If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Directions

Adults and children 6 years of age and older: Place 1 tablet into the mouth and start chewing. Swish the bubbles between your teeth for 30 seconds to 1 minute and then spit out. Rinse out the residue with water. Recommended daily usage: 1 tablet per each use, 2 to 5 uses per day. Children under 6 years of age: consult a dentist or doctor before use.

Inactive Ingredients

Sorbitol, Sodium Bicarbonate, Microcrystalline Cellulose, Lactose, Anhydrous Citric Acid, Xylitol, Sodium Lauryl Sulfate, Peppermint, Magnesium Stearate, L-Menthol, Erythritol, Sucralose, Acesulfame Potassium, Sodium Chloride

Other Information

This product is not intended to replace brushing or flossing. Store in a cool, dry place.

QUESTIONS

Call (562) 802-0131 / www.dseshopusa.com

PRINCIPAL DISPLAY PANEL

Bling:Day Bubble Candy Mouthwash - Mint Flavor

INGREDIENTS AND APPEARANCE

BLINGDAY BUBBLE CANDY SOLID MOUTHWASH 
sodium fluoride pellet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42361-081
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O)	FLUORIDE ION	0.00066 mg  in 1.1 mg

Inactive Ingredients
Ingredient Name	Strength
SORBITOL (UNII: 506T60A25R)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
SUCRALOSE (UNII: 96K6UQ3ZD4)
SODIUM BICARBONATE (UNII: 8MDF5V39QO)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
XYLITOL (UNII: VCQ006KQ1E)
PEPPERMINT (UNII: V95R5KMY2B)
MENTHOL (UNII: L7T10EIP3A)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SODIUM LAURYL SULFATE (UNII: 368GB5141J)
MAGNESIUM STEARATE (UNII: 70097M6I30)
ERYTHRITOL (UNII: RA96B954X6)
ACESULFAME POTASSIUM (UNII: 23OV73Q5G9)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 42361-081-01	16 in 1 CASE	09/09/2019
1		850 mg in 1 DOSE PACK; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part355	09/09/2019

Labeler - Dong Sung Bio Pharm. Co., Ltd. (687811661)

Registrant - Dong Sung World Wide USA, Inc. (784969219)

Establishment
Name	Address	ID/FEI	Business Operations
Dong Sung Bio Pharm. Co., Ltd.		687811661	label(42361-081)