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Diphenhydramine Hydrochloride and Hydrocortisone and Nystatin

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Overview

What is FIRST Dukes Mouthwash Compounding?

Each FIRST – Duke’s Mouthwash Compounding Kit is comprised of 0.525 grams of diphenhydramine hydrochloride powder USP, 0.06 grams of hydrocortisone powder USP, and 0.6 grams of nystatin powder USP for oral use. * FIRST – Duke’s Mouthwash Compounding Kit also contains a 236 mL suspension containing benzyl alcohol, carboxymethycellulose sodium, citric acid (anhydrous), dehydrated alcohol, FD&C yellow #5, flavors, propylene glycol, propylparaben, purified water, saccharin sodium, sodium citrate (dihydrate), and sorbitol solution. When compounded, the final product provides an homogeneous suspension containing diphenhydramine hydrochloride, hydrocortisone, and nystatin comparable to the active ingredients (diphenhydramine hydrochloride, hydrocortisone, and nystatin oral suspension) contained in



What does FIRST Dukes Mouthwash Compounding look like?



What are the available doses of FIRST Dukes Mouthwash Compounding?

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What should I talk to my health care provider before I take FIRST Dukes Mouthwash Compounding?

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How should I use FIRST Dukes Mouthwash Compounding?

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What interacts with FIRST Dukes Mouthwash Compounding?

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What are the warnings of FIRST Dukes Mouthwash Compounding?

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What are the precautions of FIRST Dukes Mouthwash Compounding?

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What are the side effects of FIRST Dukes Mouthwash Compounding?

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What should I look out for while using FIRST Dukes Mouthwash Compounding?

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What might happen if I take too much FIRST Dukes Mouthwash Compounding?

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How should I store and handle FIRST Dukes Mouthwash Compounding?

Store at 25°C (77°F); excursions permitted between 15° and 30°C (59° and 86°F) [see USP Controlled Room Temperature].10 mg tablets: NDC 49299-1090-1 bottles of 9020 mg tablets: NDC 49299-1091-2 bottles of 9040 mg tablets: NDC 49299-1092-4 bottles of 9080 mg tablets:NDC 49299-1093-8 bottles of 9010 mg tablets: NDC 49299-1090-1 bottles of 9020 mg tablets: NDC 49299-1091-2 bottles of 9040 mg tablets: NDC 49299-1092-4 bottles of 9080 mg tablets:NDC 49299-1093-8 bottles of 9010 mg tablets: NDC 49299-1090-1 bottles of 9020 mg tablets: NDC 49299-1091-2 bottles of 9040 mg tablets: NDC 49299-1092-4 bottles of 9080 mg tablets:NDC 49299-1093-8 bottles of 9010 mg tablets: NDC 49299-1090-1 bottles of 9020 mg tablets: NDC 49299-1091-2 bottles of 9040 mg tablets: NDC 49299-1092-4 bottles of 9080 mg tablets:NDC 49299-1093-8 bottles of 9010 mg tablets: NDC 49299-1090-1 bottles of 9020 mg tablets: NDC 49299-1091-2 bottles of 9040 mg tablets: NDC 49299-1092-4 bottles of 9080 mg tablets:NDC 49299-1093-8 bottles of 9010 mg tablets: NDC 49299-1090-1 bottles of 9020 mg tablets: NDC 49299-1091-2 bottles of 9040 mg tablets: NDC 49299-1092-4 bottles of 9080 mg tablets:NDC 49299-1093-8 bottles of 9010 mg tablets: NDC 49299-1090-1 bottles of 9020 mg tablets: NDC 49299-1091-2 bottles of 9040 mg tablets: NDC 49299-1092-4 bottles of 9080 mg tablets:NDC 49299-1093-8 bottles of 9010 mg tablets: NDC 49299-1090-1 bottles of 9020 mg tablets: NDC 49299-1091-2 bottles of 9040 mg tablets: NDC 49299-1092-4 bottles of 9080 mg tablets:NDC 49299-1093-8 bottles of 90


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Clinical Information

Chemical Structure

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Clinical Pharmacology

Non-Clinical Toxicology
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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).