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Sodium Fluoride

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Overview

What is DentiCare Pro-Rinse?

Medicom

DentiCare Pro-Rinse

2% Neutral Sodium Fluoride Oral Rinse

NDC 64778-1443-1

10044-MM



What does DentiCare Pro-Rinse look like?



What are the available doses of DentiCare Pro-Rinse?

Sorry No records found.

What should I talk to my health care provider before I take DentiCare Pro-Rinse?

Sorry No records found

How should I use DentiCare Pro-Rinse?

Topical anti-caries solution. Neutral pH is safe for patients with crowns and restorations. Dispense 10 mL of slution into a measuring cup. Instruct patient to rinse vigorously for 60 seconds, around and in between teeth, then expectorate. For maximun benefit, repeat the rinse procedure with additional 10 mL. 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.


What interacts with DentiCare Pro-Rinse?

Sorry No Records found


What are the warnings of DentiCare Pro-Rinse?

Sorry No Records found


What are the precautions of DentiCare Pro-Rinse?

Sorry No Records found


What are the side effects of DentiCare Pro-Rinse?

Sorry No records found


What should I look out for while using DentiCare Pro-Rinse?


What might happen if I take too much DentiCare Pro-Rinse?

Sorry No Records found


How should I store and handle DentiCare Pro-Rinse?

Sorry No Records found


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Clinical Information

Chemical Structure

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Clinical Pharmacology

Non-Clinical Toxicology












      Taking theophylline extended-release tablets immediately after ingesting a high fat content meal (45 g fat, 55 g carbohydrates, 28 g protein, 789 calories) may result in a somewhat higher C and delayed T and a somewhat greater extent of absorption when compared to taking it in the fasting state. The influence of the type and amount of other foods, as well as the time interval between drug and food, has not been studied.  Most serum theophylline assays in clinical use are immunoassays which are specific for theophylline. Other xanthines such as caffeine, dyphylline, and pentoxifylline are not detected by these assays. Some drugs (e.g.,cefazolin, cephalothin), however, may interfere with certain HPLC techniques. Caffeine and xanthine metabolites in neonates or patients with renal dysfunction may cause the reading from some dry reagent office methods to be higher than the actual serum theophylline concentration. 

Keep out 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 40C or 104F. 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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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).