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BON SCENT Sparkling Tooth Wash

Medically reviewed by Drugs.com. Last updated on Apr 7, 2021.

Dosage form: tablet
Ingredients: Sodium Fluoride 9.38mg in 853mg
Labeler: Lucella Co.,ltd
NDC Code: 72869-010

ACTIVE INGREDIENT

Active ingredients: Sodium Fluoride 1.1%

INACTIVE INGREDIENT

Inactive ingredients:


DL-Malic acid, DL-Camphor, Glyceryl Monostearate, Glycyrrhizinic acid, Sodium Lauroyl Sarcosinate, Mannitol, Menthol, peppermint oil, Sodium Saccharin dihydrate, Magnesium stearate, Xylitol, Tricalcium phosphate, Calcium Carbonate, Colloid Silica, Sodium bicarbonate, PEG-150, Enzymatically Modified Stevia, Hydroxypropylmethylcellulose

PURPOSE

Purpose: Anticaries & Anticavity

WARNINGS

Warnings:


- Keep in a cool and dry place.
- Do not swallow.
- The fluorine content is 583.21ppm. (Total content should be less than 1,000ppm)
- If a child under 6 years of age swallowed large quantities, consult a physician or dentist immediately.
- Keep out of the reach of children under 6 years.

KEEP OUT OF REACH OF CHILDREN

Keep out of the reach of children under 6 years.

Uses

Uses:
Helps protect against cavities

Directions

Directions:
- Put 1 tablet into your mouth and wash your gums, teeth, and tongue using your tongue and lips.
-Lastly rinse several times with water.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BON SCENT SPARKLING TOOTH WASH 
sodium fluoride tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72869-010
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Sodium Fluoride (FLUORIDE ION) FLUORIDE ION9.38 mg  in 853 mg
Inactive Ingredients
Ingredient NameStrength
Mannitol 
Menthol 
Product Characteristics
ColorwhiteScoreno score
ShapeROUNDSize12mm
FlavorPEPPERMINTImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:72869-010-0230 BLISTER PACK in 1 POUCH
1NDC:72869-010-01853 mg in 1 BLISTER PACK
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35501/02/2019
Labeler - Lucella Co.,ltd (694733285)
Registrant - Lucella Co.,ltd (694733285)
Establishment
NameAddressID/FEIOperations
EQMAXON Corp.557821534manufacture(72869-010)

Document Id: d95e5a00-3461-47a5-ab94-ae8f33864e65
Set id: a8a409c7-a3c2-49c0-91df-052f2a7a08b3
Version: 2
Effective Time: 20190417
 
Lucella Co.,ltd

Further information

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

Medical Disclaimer