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Kosette salt tooth - Medication Information

Product NDC Code 74724-0010
Drug Name

Kosette salt tooth

Type Brand
Active Ingredients
Sodium monofluorophosphate .76 g/100g
Route DENTAL
Dosage Form PASTE, DENTIFRICE
RxCUI drug identifier 545626
Application Number part355
Labeler Name K.Boeun Pharmaceutical Co.,Ltd.
Packages
Package NDC Code Description
74724-0010-1 100 g in 1 tube (74724-0010-1)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
SODIUM MONOFLUOROPHOSPHATE

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
For dental use only

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
D-Sorbitol Solution, WATER, SILICON DIOXIDE, CONCENTRATED GLYCERIN, SODIUM COCOYL GLUTAMATE, POLYETHYLENE GLYCOL 1500, CARBOXYMETHYLCELLULOSE SODIUM, PEPPERMINT OIL, ACTIVE CARBON, L-MENTHOL, CITRUS PARADISI (GRAPEFRUIT) SEED EXTRACT, XYLITOL, SODIUM CHLORIDE, ENZYMATICALLY MODIFIED STEVIA, CHAMOMILLA RECUTITA (MATRICARIA) FLOWER EXTRACT, ALOE EXTRACT, SAGE EXTRACT

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Brush teeth thoroughly for at least one minute, preferably after each meal or at least twice a day (morning and evening) or as recommended by a dentist or physician

Purpose

Information about the drug product’s indications for use.
ANTI-CAVITY

Spl product data elements

Usually a list of ingredients in a drug product.
Kosette Salt Tooth SODIUM MONOFLUOROPHOSPHATE WATER SODIUM MONOFLUOROPHOSPHATE FLUORIDE ION SILICON DIOXIDE SORBITOL XYLITOL

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
1

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep out of reach of children

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
Storage method 1. Keep it at room temperature in a classified container. 2. Cover and store at room temperature. 3. Store in a not moisture and cool place. 4. Air may come out during use of this product, but there is no problem with its weight. Usage Precautions 1. Be careful not to swallow. Rinse mouth thoroughly after use 2. If the use of toothpaste causes abnormalities such as gums or mouth injury, discontinue use and consult a doctor or dentist. 3. For children under 6 years of age, use a small amount of toothpaste as small as pea per use, and use under the guidance of a guardian to avoid sucking or swallowing. 4. If a child under 6 years old swallows large amount, consult with a doctor or dentist immediately. 5. Keep out of the reach of children under 6 years of age.

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API