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Kerydin

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Overview

What is Kerydin?

KERYDIN (tavaborole) topical solution, 5% contains tavaborole, 5% (w/w) in a clear, colorless alcohol-based solution for topical use. The active ingredient, tavaborole, is an oxaborole antifungal with the chemical name of 5-fluoro-1,3-dihydro-1-hydroxy-2,1-benzoxaborole. The chemical formula is CHBFO, the molecular weight is 151.93 and the structural formula is:

Tavaborole is a white to off-white powder. It is slightly soluble in water and freely soluble in ethanol and propylene glycol.

Each mL of KERYDIN contains 43.5 mg of tavaborole. Inactive ingredients include alcohol, edetate calcium disodium, and propylene glycol.



What does Kerydin look like?



What are the available doses of Kerydin?

Solution, 5%. ()

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

How should I use Kerydin?

KERYDIN (tavaborole) topical solution, 5% is an oxaborole antifungal indicated for the treatment of onychomycosis of the toenails due to or .

Apply KERYDIN to affected toenails once daily for 48 weeks.KERYDIN should be applied to the entire toenail surface and under the tip of each toenail being treated.KERYDIN is for topical use only and not for oral, ophthalmic, or intravaginal use.


What interacts with Kerydin?

Sorry No Records found


What are the warnings of Kerydin?

Sorry No Records found


What are the precautions of Kerydin?

Sorry No Records found


What are the side effects of Kerydin?

Sorry No records found


What should I look out for while using Kerydin?

None.


What might happen if I take too much Kerydin?

Sorry No Records found


How should I store and handle Kerydin?

Store at 20–25°C (68–77°F); excursions permitted to 15–30°C (59–86°F) [see USP Controlled Room Temperature].CAUTION: Flammable. Keep away from heat and flame.Discard product within 3 months after insertion of the dropper.Keep bottle tightly closed. Keep out of reach of children.Concentrated Zinc Sulfate Injection, USP, 5 mg zinc/mLNDC 0517-8105-25     5 mL Vials     Packed in a box of 25Store 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).AMERICANREGENT, INC.SHIRLEY, NY 11967IN8105Rev. 1/09MG #14229Concentrated Zinc Sulfate Injection, USP, 5 mg zinc/mLNDC 0517-8105-25     5 mL Vials     Packed in a box of 25Store 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).AMERICANREGENT, INC.SHIRLEY, NY 11967IN8105Rev. 1/09MG #14229Concentrated Zinc Sulfate Injection, USP, 5 mg zinc/mLNDC 0517-8105-25     5 mL Vials     Packed in a box of 25Store 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).AMERICANREGENT, INC.SHIRLEY, NY 11967IN8105Rev. 1/09MG #14229Concentrated Zinc Sulfate Injection, USP, 5 mg zinc/mLNDC 0517-8105-25     5 mL Vials     Packed in a box of 25Store 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).AMERICANREGENT, INC.SHIRLEY, NY 11967IN8105Rev. 1/09MG #14229Concentrated Zinc Sulfate Injection, USP, 5 mg zinc/mLNDC 0517-8105-25     5 mL Vials     Packed in a box of 25Store 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).AMERICANREGENT, INC.SHIRLEY, NY 11967IN8105Rev. 1/09MG #14229Concentrated Zinc Sulfate Injection, USP, 5 mg zinc/mLNDC 0517-8105-25     5 mL Vials     Packed in a box of 25Store 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).AMERICANREGENT, INC.SHIRLEY, NY 11967IN8105Rev. 1/09MG #14229Concentrated Zinc Sulfate Injection, USP, 5 mg zinc/mLNDC 0517-8105-25     5 mL Vials     Packed in a box of 25Store 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).AMERICANREGENT, INC.SHIRLEY, NY 11967IN8105Rev. 1/09MG #14229Concentrated Zinc Sulfate Injection, USP, 5 mg zinc/mLNDC 0517-8105-25     5 mL Vials     Packed in a box of 25Store 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).AMERICANREGENT, INC.SHIRLEY, NY 11967IN8105Rev. 1/09MG #14229


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Clinical Information

Chemical Structure

No Image found
Clinical Pharmacology

KERYDIN is an oxaborole antifungal [see ].

Non-Clinical Toxicology
None.

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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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