Skip to main content

Blingday Bubble Candy Solid Mouthwash

Medically reviewed by Drugs.com. Last updated on Aug 30, 2021.

Dosage form: pellet
Ingredients: SODIUM FLUORIDE 0.00066mg in 1.1mg
Labeler: Dong Sung Bio Pharm. Co., Ltd.
NDC Code: 42361-081

42361-081-01 Drug Facts

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.

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

Bling:Day Bubble Candy Mouthwash - Mint Flavor

BLINGDAY BUBBLE CANDY SOLID MOUTHWASH 
sodium fluoride pellet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:42361-081
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM FLUORIDE (FLUORIDE ION) FLUORIDE ION0.00066 mg  in 1.1 mg
Inactive Ingredients
Ingredient NameStrength
SORBITOL 
MICROCRYSTALLINE CELLULOSE 
ANHYDROUS LACTOSE 
SUCRALOSE 
SODIUM BICARBONATE 
ANHYDROUS CITRIC ACID 
XYLITOL 
PEPPERMINT 
MENTHOL 
SODIUM CHLORIDE 
SODIUM LAURYL SULFATE 
MAGNESIUM STEARATE 
ERYTHRITOL 
ACESULFAME POTASSIUM (ACESULFAME)  
Packaging
#Item CodePackage Description
1NDC:42361-081-0116 DOSE PACK in 1 CASE
1850 mg in 1 DOSE PACK
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35509/09/2019
Labeler - Dong Sung Bio Pharm. Co., Ltd. (687811661)
Registrant - Dong Sung World Wide USA, Inc. (784969219)
Establishment
NameAddressID/FEIOperations
Dong Sung Bio Pharm. Co., Ltd.687811661label(42361-081)

 
Dong Sung Bio Pharm. Co., Ltd.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.