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Denti-Care Denti-Pro

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Overview

What is Denti-Care Denti-Pro?

Medicom

Denti-Care

Denti-Pro 60 Sec Gel

2.72 % Topical Sodium Fluoride Gel

60 Second Application (1.23 % fluoride ions)

Raspberry

16.23 fl oz / 480mL

NDC 64778-0218-1

NPN 80008336

Item code 10021-RB



What does Denti-Care Denti-Pro look like?



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

Sorry No records found.

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

Sorry No records found

How should I use Denti-Care Denti-Pro?

A topical anti-caries preparation. Optimized low pH for penetration. Ideal thixotropic action. Artificially flavoured.

Directions:

1. Use after thorough prophylaxis

2. To dispense, fill tray(s) 1/3 with gel

3. Insert tray(s) in mouth and have patient bite down lightly for 60 seconds

4. Remove tray(s) and have patient expectorate excess

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

Medicinal ingredients: Fluoride ions 1.23 % w/w (from 2.72 % w/w sodium fluoride)


What interacts with Denti-Care Denti-Pro?

Sorry No Records found


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

Sorry No Records found


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

Sorry No Records found


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

Sorry No records found


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


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

Sorry No Records found


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

Sorry No Records found


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Clinical Information

Chemical Structure

No Image found
Clinical Pharmacology

Non-Clinical Toxicology
Drug Interactions.

I. Due to the competition of salicylate with other drugs for binding to serum albumin the following drug interactions may occur:

II. Drugs changing salicylate levels by altering renal tubular reabsorption:

III. Drugs with complicated interactions with salicylates:

The following alterations of laboratory tests have been reported during salicylate therapy:

Warnings: KEEP OUT OF REACH OF CHILDREN. For professional use only. Do not swallow.

Not recommended for use by children under 18 months of age.

Store at room temperature. Do not expose to excessive heat over 40 degrees C or 104 degrees F.

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

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