Skip to main content

MIPaste ONE

Dosage form: paste, dentifrice
Ingredients: SODIUM FLUORIDE 0.0024g in 1g, POTASSIUM NITRATE 0.06g in 1g
Labeler: GC America Inc.
NDC code: 61596-437

Medically reviewed by Drugs.com. Last updated on Jan 10, 2024.

Active Ingredient

Sodium fluoride

0.24% w/w Anti-cavity

Potassium nitrate

5% (w/w)* Anti-sensitivity

*Maximum FDA sensitivity active ingredient

Use

-aids in the prevention of dental cavities

-builds increasing protection against painful sensitivity of the teeth to cold, heat, acids, sweets or contact

Warning

Warning If the sensitivity persists after 4 weeks of use, consult a dentist or physician. Keep out of reach of children. If more than the recommended amount of paste used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away. Do not use on patients with a milk protein and/or hydroxybenzoates allergy. In case of allergic reaction, stop use, rinse mouth with water and seek medical advice.

Directions

For adults and children 12 years of age or older, apply a small, pea-sized amount of MI Paste One to your toothbrush. For best results, brush for 2 minutes, expectorate and do not rinse; use twice a day. Replace cap after use. For children under 12 years of age, consult a dentist or physician.

Inactive ingredient

Pure water, Glycerol, RECALDENT TM (CPP-ACP) Casein Phosphopeptide-Amorphous Calcium Phosphate, Sorbitol, CMC-Na, Propylene glycol, Silicon dioxide, Titanium dioxide, Xylitol, Phosphoric acid, flavoring, Methyl salicylate, Sodium saccharin, Ethyl p-hydroxybenzoate, Propyl p-hydroxybenzoate, Butyl p-hydroxybenzoate, Sodium-N-lauroyl sarcosinate

Question or comments

1-708-323-7063 www.gcamerica.com

Warning

Keep out of reach of children.

Anti-cavity toothpaste with bio-available calcium.

Anti-cavity

Rebuilds enamel

Helps against sensitivity

Sodium Fluoride 0.24% w/w (1,100ppmF)

Potassium Nitrate 5% w/w/

Tube box

Tube

MIPASTE  ONE
sodium fluoride, potassium nitrate paste, dentifrice
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:61596-437
Route of AdministrationDENTALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SODIUM FLUORIDE (FLUORIDE ION) FLUORIDE ION0.0024 g  in 1 g
POTASSIUM NITRATE (NITRATE ION) POTASSIUM NITRATE0.06 g  in 1 g
Inactive Ingredients
Ingredient NameStrength
SILICON DIOXIDE 
SORBITOL 
PROPYLENE GLYCOL 
XYLITOL 
PHOSPHORIC ACID 
TITANIUM DIOXIDE 
ETHYLPARABEN 
BUTYLPARABEN 
SACCHARIN SODIUM 
PROPYLPARABEN 
WATER 
GLYCERIN 
SODIUM LAUROYL SARCOSINATE 
METHYL SALICYLATE 
CALCIUM PHOSPHATE 
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM 
Product Characteristics
Color    Score    
ShapeSize
FlavorMINTImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:61596-437-411 TUBE in 1 BOX
1NDC:61596-437-4046 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35607/03/2017
Labeler - GC America Inc. (005473608)
Establishment
NameAddressID/FEIOperations
GC America Inc.005473608manufacture(61596-437)

Revised: 01/2020
 
GC America Inc.

Further information

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