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azelaic acid

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Overview

What is FINACEA FOAM?

Finacea (azelaic acid) Foam contains 15% (w/w) azelaic acid, a naturally-occurring saturated dicarboxylic acid and is suspended in an oil-in-water emulsion vehicle for topical administration to affected skin area. Chemically, azelaic acid is 1,7-heptanedicarboxylic acid. The structural formula of azelaic acid is:

Azelaic acid has a molecular formula of C H O and a molecular weight of 188.22.

The aluminum containers are filled with hydrophilic emulsion, crimped with a continuous spray valve, and pressurized with propellants consisting of propane, butane, and isobutane. Each gram of Finacea Foam contains 0.15 g of azelaic acid. Finacea Foam also contains benzoic acid, cetostearyl alcohol, dimethyl isosorbide, medium-chain triglycerides, methylcellulose, mono- and di-glycerides, polyoxyl 40 stearate, polysorbate 80, propylene glycol, purified water, sodium hydroxide, and xanthan gum as inactive ingredients.



What does FINACEA FOAM look like?



What are the available doses of FINACEA FOAM?

Foam, 15% ()

What should I talk to my health care provider before I take FINACEA FOAM?

How should I use FINACEA FOAM?

Finacea(azelaic acid) Foam, 15% is indicated for topical treatment of the inflammatory papules and pustules of mild to moderate rosacea.

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What interacts with FINACEA FOAM?

Sorry No Records found


What are the warnings of FINACEA FOAM?

Sorry No Records found


What are the precautions of FINACEA FOAM?

Sorry No Records found


What are the side effects of FINACEA FOAM?

Sorry No records found


What should I look out for while using FINACEA FOAM?

None.


What might happen if I take too much FINACEA FOAM?

Sorry No Records found


How should I store and handle FINACEA FOAM?

Store at 20° to 25°C (68° to 77°F); excursions permitted to 15° to 30°C (59° to 86°F) [See USP Controlled Room Temperature]. Keep tightly closed (protect from moisture). Protect from light.Product: 50436-5620NDC: 50436-5620-1 30 TABLET in a BOTTLENDC: 50436-5620-2 60 TABLET in a BOTTLEProduct: 50436-5620NDC: 50436-5620-1 30 TABLET in a BOTTLENDC: 50436-5620-2 60 TABLET in a BOTTLEProduct: 50436-5620NDC: 50436-5620-1 30 TABLET in a BOTTLENDC: 50436-5620-2 60 TABLET in a BOTTLE


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Clinical Information

Chemical Structure

No Image found
Clinical Pharmacology

Non-Clinical Toxicology
None.

Centrally Acting Agents

Alcohol

Antacids

Compounds Which Inhibit Certain Hepatic Enzymes

Phenytoin

There have been isolated reports of hypopigmentation after use of azelaic acid. Because azelaic acid has not been well studied in patients with dark complexion, monitor these patients for early signs of hypopigmentation.

The following adverse reactions are described elsewhere in the prescribing information:

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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

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