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| Product NDC Code | 74724-0025 | ||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| Drug Name | Saltrain tooth |
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| Type | Brand | ||||||||||
| Pharm Class | Antifibrinolytic Agent [EPC], Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Decreased Fibrinolysis [PE], Increased Coagulation Factor Activity [PE] |
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| Active Ingredients |
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| Route | DENTAL | ||||||||||
| Dosage Form | PASTE, DENTIFRICE | ||||||||||
| Labeler Name | K.Boeun Pharmaceutical Co.,Ltd. | ||||||||||
| Packages |
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| Check if available Online | Get Medication Prices online with Discount |
Active ingredient
A list of the active, medicinal ingredients in the drug product.Sodium Monofluorophosphate, Precipitated Calcium Carbonate, Dibasic Calcium Phosphate, Aminocaproic Acid, Aluminium Chlorohydroxy Allantoinate
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 Concentrated Glycerin Polyethylene Glycol 1500 Xanthangum Sodium Cocoyl Glutamate Silicon Dioxide Titanium Oxide Enzymatically Modified Stevia Xylitol Sodium Chloride Ascorbic Acid Mentha Oil l-Menthol Spearmint Oil Water
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.Apply an appropriate amount to your toothbrush and brush your teeth by brushing.
Purpose
Information about the drug product’s indications for use.For dental care
Spl product data elements
Usually a list of ingredients in a drug product.SALTRAIN TOOTH Sodium monofluorophosphate, Precipitated Calcium Carbonate, Dibasic Calcium Phosphate, Aminocaproic Acid, Aluminium Chlorohydroxy Allantoinate SODIUM MONOFLUOROPHOSPHATE FLUORIDE ION CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS XYLITOL WATER CALCIUM CARBONATE CALCIUM CATION ALCLOXA ALCLOXA AMINOCAPROIC ACID AMINOCAPROIC ACID
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.Warnings Keep out of reach of children ■ If more than used for rinsing is accidentally swallowed, get medical help or contact a Poison Control Center right away. Other Information ■ Store in an airtight container at room temperature ■ Date of use : 36 months from the date of manufacture
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