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Sodium Fluoride

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Overview

What is Denti-Care Denti-Rinse?

AMD Medicom Inc.

DentiCare Pro-Rinse

2% Neutral Sodium Fluoride Oral Rinse

Berry

1.9 L / 64 fl oz

NDC 64778-0448-1

NPN 80008542

Rx Only in US

Item code 10044-B



What does Denti-Care Denti-Rinse look like?



What are the available doses of Denti-Care Denti-Rinse?

Sorry No records found.

What should I talk to my health care provider before I take Denti-Care Denti-Rinse?

Sorry No records found

How should I use Denti-Care Denti-Rinse?

Directions: Dispense 10mL of solution into a measuring cup. Instruct patient to rinse vigorously for 60 seconds, around and in between teeth, then expectorate. For maximum benefit repeat the rinse procedure with an additional 10mL

Advise patient not to eat, drink or rinse for 30 minutes after application

Pro-Rinse solution may also be applied with a cotton tip applicator to teeth isolated with cotton rolls

Medicinal ingredients: Sodium fluoride 2.0% w/w


What interacts with Denti-Care Denti-Rinse?

Sorry No Records found


What are the warnings of Denti-Care Denti-Rinse?

Sorry No Records found


What are the precautions of Denti-Care Denti-Rinse?

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What are the side effects of Denti-Care Denti-Rinse?

Sorry No records found


What should I look out for while using Denti-Care Denti-Rinse?


What might happen if I take too much Denti-Care Denti-Rinse?

Sorry No Records found


How should I store and handle Denti-Care Denti-Rinse?

Sorry No Records found


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Clinical Information

Chemical Structure

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Clinical Pharmacology

Non-Clinical Toxicology
The pharmacokinetic interactions listed below are potentially clinically important. Mutual inhibition of metabolism occurs with concurrent use of cyclosporin and methylprednisolone; therefore, it is possible that adverse events associated with the individual use of either drug may be more apt to occur. Convulsions have been reported with concurrent use of methylprednisolone and cyclosporin. Drugs that induce hepatic enzymes such as phenobarbital, phenytoin and rifampin may increase the clearance of methylprednisolone and may require increases in methylprednisolone dose to achieve the desired response. Drugs such as troleandomycin and ketoconazole may inhibit the metabolism of methylprednisolone and thus decrease its clearance. Therefore, the dose of methylprednisolone should be titrated to avoid steroid toxicity.

Methylprednisolone may increase the clearance of chronic high dose aspirin. This could lead to decreased salicylate serum levels or increase the risk of salicylate toxicity when methylprednisolone is withdrawn. Aspirin should be used cautiously in conjunction with corticosteroids in patients suffering from hypoprothrombinemia.

The effect of methylprednisolone on oral anticoagulants is variable. There are reports of enhanced as well as diminished effects of anticoagulant when given concurrently with corticosteroids. Therefore, coagulation indices should be monitored to maintain the desired anticoagulant effect.

KEEP OUT OF REACH OF CHILDREN. For professional use only

Not recommended for use by children under 6 years of age. Do not swallow

Store at room temperature. Do not expose to excessive heat over 40ºC or 104ºF

Do not use if seal is broken

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Reference

This information is obtained from the National Institute of Health's Standard Packaging Label drug database.
"https://dailymed.nlm.nih.gov/dailymed/"

While we update our database periodically, we cannot guarantee it is always updated to the latest version.

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Professional

Clonazepam Description Each single-scored tablet, for oral administration, contains 0.5 mg, 1 mg, or 2 mg Clonazepam, USP, a benzodiazepine. Each tablet also contains corn starch, lactose monohydrate, magnesium stearate, microcrystalline cellulose, and povidone. Clonazepam tablets USP 0.5 mg contain Yellow D&C No. 10 Aluminum Lake. Clonazepam tablets USP 1 mg contain Yellow D&C No. 10 Aluminum Lake, as well as FD&C Blue No. 1 Aluminum Lake. Chemically, Clonazepam, USP is 5-(o-chlorophenyl)-1,3-dihydro-7-nitro-2H-1,4-benzodiazepin-2-one. It is a light yellow crystalline powder. It has the following structural formula: C15H10ClN3O3 M.W. 315.72
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Tips

Tips

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Interactions

Interactions

A total of 440 drugs (1549 brand and generic names) are known to interact with Imbruvica (ibrutinib). 228 major drug interactions (854 brand and generic names) 210 moderate drug interactions (691 brand and generic names) 2 minor drug interactions (4 brand and generic names) Show all medications in the database that may interact with Imbruvica (ibrutinib).