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Multivitamin with fluoride

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Overview

What is Multivitamin with fluoride?

Off-white to pale yellow, speckled, fruit flavor, round-shaped chewable tablet debossed "SCI" on one side and "5" on the other.



What does Multivitamin with fluoride look like?



What are the available doses of Multivitamin with fluoride?

Sorry No records found.

What should I talk to my health care provider before I take Multivitamin with fluoride?

Sorry No records found

How should I use Multivitamin with fluoride?

USE AS DIRECTED BY YOUR PHYSICIAN.


What interacts with Multivitamin with fluoride?

Sorry No Records found


What are the warnings of Multivitamin with fluoride?

Sorry No Records found


What are the precautions of Multivitamin with fluoride?

Sorry No Records found


What are the side effects of Multivitamin with fluoride?

Sorry No records found


What should I look out for while using Multivitamin with fluoride?

KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN. IF OVERDOSAGE IS SUSPECTED, SEEK PROFESSIONAL ASSISTANCE OR CONTACT A POISON CONTROL CENTER IMMEDIATELY 1-800-222-1222. TABLET SHOULD BE CHEWED. THIS PRODUCT, AS WITH ALL CHEWABLE TABLETS, IS NOT RECOMMENDED FOR CHILDREN UNDER AGE 4 DUE TO RISK OF CHOKING.

DO NOT USE IF FOIL SEAL UNDER CAP IS BROKEN OR MISSING


What might happen if I take too much Multivitamin with fluoride?

Sorry No Records found


How should I store and handle Multivitamin with fluoride?

Dispense in a well-closed container as defined in the USP.Keep container tightly closed.  Protect from light, moisture, and freezing, -20°C (-4°F).Store at 20-25°C (68-77°F) [See USP Controlled Room Temperature].Manufactured by:Actavis Elizabeth LLCElizabeth, NJ 07207 USADistributed by:Actavis Pharma, Inc.Parsippany, NJ 07054 USAMarketed/ Packaged by: Camarillo, CA 93012 USA40-9176Revised — November 2015Dispense in a well-closed container as defined in the USP.Keep container tightly closed.  Protect from light, moisture, and freezing, -20°C (-4°F).Store at 20-25°C (68-77°F) [See USP Controlled Room Temperature].Manufactured by:Actavis Elizabeth LLCElizabeth, NJ 07207 USADistributed by:Actavis Pharma, Inc.Parsippany, NJ 07054 USAMarketed/ Packaged by: Camarillo, CA 93012 USA40-9176Revised — November 2015Dispense in a well-closed container as defined in the USP.Keep container tightly closed.  Protect from light, moisture, and freezing, -20°C (-4°F).Store at 20-25°C (68-77°F) [See USP Controlled Room Temperature].Manufactured by:Actavis Elizabeth LLCElizabeth, NJ 07207 USADistributed by:Actavis Pharma, Inc.Parsippany, NJ 07054 USAMarketed/ Packaged by: Camarillo, CA 93012 USA40-9176Revised — November 2015Dispense in a well-closed container as defined in the USP.Keep container tightly closed.  Protect from light, moisture, and freezing, -20°C (-4°F).Store at 20-25°C (68-77°F) [See USP Controlled Room Temperature].Manufactured by:Actavis Elizabeth LLCElizabeth, NJ 07207 USADistributed by:Actavis Pharma, Inc.Parsippany, NJ 07054 USAMarketed/ Packaged by: Camarillo, CA 93012 USA40-9176Revised — November 2015Dispense in a well-closed container as defined in the USP.Keep container tightly closed.  Protect from light, moisture, and freezing, -20°C (-4°F).Store at 20-25°C (68-77°F) [See USP Controlled Room Temperature].Manufactured by:Actavis Elizabeth LLCElizabeth, NJ 07207 USADistributed by:Actavis Pharma, Inc.Parsippany, NJ 07054 USAMarketed/ Packaged by: Camarillo, CA 93012 USA40-9176Revised — November 2015Dispense in a well-closed container as defined in the USP.Keep container tightly closed.  Protect from light, moisture, and freezing, -20°C (-4°F).Store at 20-25°C (68-77°F) [See USP Controlled Room Temperature].Manufactured by:Actavis Elizabeth LLCElizabeth, NJ 07207 USADistributed by:Actavis Pharma, Inc.Parsippany, NJ 07054 USAMarketed/ Packaged by: Camarillo, CA 93012 USA40-9176Revised — November 2015Dispense in a well-closed container as defined in the USP.Keep container tightly closed.  Protect from light, moisture, and freezing, -20°C (-4°F).Store at 20-25°C (68-77°F) [See USP Controlled Room Temperature].Manufactured by:Actavis Elizabeth LLCElizabeth, NJ 07207 USADistributed by:Actavis Pharma, Inc.Parsippany, NJ 07054 USAMarketed/ Packaged by: Camarillo, CA 93012 USA40-9176Revised — November 2015Dispense in a well-closed container as defined in the USP.Keep container tightly closed.  Protect from light, moisture, and freezing, -20°C (-4°F).Store at 20-25°C (68-77°F) [See USP Controlled Room Temperature].Manufactured by:Actavis Elizabeth LLCElizabeth, NJ 07207 USADistributed by:Actavis Pharma, Inc.Parsippany, NJ 07054 USAMarketed/ Packaged by: Camarillo, CA 93012 USA40-9176Revised — November 2015Product: 50090-0435NDC: 50090-0435-1 100 TABLET, CHEWABLE in a BOTTLE, PLASTIC Product: 50090-0435NDC: 50090-0435-1 100 TABLET, CHEWABLE in a BOTTLE, PLASTIC


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Clinical Information

Chemical Structure

No Image found
Clinical Pharmacology

Non-Clinical Toxicology
KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN. IF OVERDOSAGE IS SUSPECTED, SEEK PROFESSIONAL ASSISTANCE OR CONTACT A POISON CONTROL CENTER IMMEDIATELY 1-800-222-1222. TABLET SHOULD BE CHEWED. THIS PRODUCT, AS WITH ALL CHEWABLE TABLETS, IS NOT RECOMMENDED FOR CHILDREN UNDER AGE 4 DUE TO RISK OF CHOKING.

DO NOT USE IF FOIL SEAL UNDER CAP IS BROKEN OR MISSING

Administration of reserpine during therapy with a tricyclic antidepressant has been shown to produce a “stimulating” effect in some depressed patients.

Close supervision and careful adjustment of the dosage are required when nortriptyline hydrochloride is used with other anticholinergic drugs and sympathomimetic drugs.

Concurrent administration of cimetidine and tricyclic antidepressants can produce clinically significant increases in the plasma concentrations of the tricyclic antidepressant. The patient should be informed that the response to alcohol may be exaggerated.

A case of significant hypoglycemia has been reported in a type II diabetic patient maintained on chlorpropamide (250 mg/day), after the addition of nortriptyline (125 mg/day).





In addition, certain drugs inhibit the activity of this isozyme and make normal metabolizers resemble poor metabolizers. An individual who is stable on a given dose of TCA may become abruptly toxic when given one of these inhibiting drugs as concomitant therapy. The drugs that inhibit cytochrome P450 2D6 include some that are not metabolized by the enzyme (quinidine; cimetidine) and many that are substrates for P450 2D6 (many other antidepressants, phenothiazines, and the Type 1C antiarrhythmics propafenone and flecainide). While all the selective serotonin reuptake inhibitors (SSRIs), e.g., fluoxetine, sertraline, and paroxetine, inhibit P450 2D6, they may vary in the extent of inhibition. The extent to which SSRI TCA interactions may pose clinical problems will depend on the degree of inhibition and the pharmacokinetics of the SSRI involved. Nevertheless, caution is indicated in the coadministration of TCAs with any of the SSRIs and also in switching from one class to the other. Of particular importance, sufficient time must elapse before initiating TCA treatment in a patient being withdrawn from fluoxetine, given the long half-life of the parent and active metabolite (at least 5 weeks may be necessary).

Concomitant use of tricyclic antidepressants with drugs that can inhibit cytochrome P450 2D6 may require lower doses than usually prescribed for either the tricyclic antidepressant or the other drug. Furthermore, whenever one of these other drugs is withdrawn from co-therapy, an increased dose of tricyclic antidepressant may be required. It is desirable to monitor TCA plasma levels whenever a TCA is going to be coadministered with another drug known to be an inhibitor of P450 2D6.

















Do not use this product if you are allergic to any of the ingredients. Take this product at least 2 hours before or after taking any products containing calcium (including milk, yogurt, other dairy products) or aluminum/magnesium hydroxide (e.g., certain antacids/laxatives). Prolonged daily ingestion of excessive fluoride may result in varying degrees of dental fluorosis. Account for all daily sources of fluoride intake.

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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).