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Denpo cavity prevention

Medically reviewed on Mar 19, 2018

Dosage form: tablet, chewable
Ingredients: SODIUM FLUORIDE 1.1mg
Labeler: Suheung Capsule Co., Ltd
NDC Code: 52146-1001

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.

Drug Facts

Active ingredient: Sodium Fluoride

Benefits / Effects
(1) cavity prevention
(2) removal of bad breath, cleaning of oral cavity

Directions / dosage
(1) direction
take and chew one tablet, and clean teeth and gums using tongue and lips, rinse out with water
(2) dosage
2~5 times per day

Caution
(1) avoid direct sunlight, store in a cool dry place
(2) do not swallow

Warning
(1) the fluoride content of this product is 597.46 ppm (total fluoride content needs to be below 1,000 ppm)
(2) for children under six, use a pea-sized amount per use, do not eat or swallow
(3) immediately contact a physician if a child under six has swallowed a large portion
(4) keep and store away from children under six

DENPO  CAVITY PREVENTION
fluoride tablet, chewable
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52146-1001
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM FLUORIDE (FLUORIDE ION) SODIUM FLUORIDE1.1 mg
Product Characteristics
Colorpink (white pink) Scoreno score
ShapeROUND (none) Size14mm
FlavorImprint Code3;hp;x
Contains    
Packaging
#Item CodePackage Description
1NDC:52146-1001-160 TABLET, CHEWABLE (TABLET) in 1 PACKAGE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other03/18/2010
Labeler - Suheung Capsule Co., Ltd (687943324)

 
Suheung Capsule Co., Ltd

Further information

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

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