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Guaiacol and Eugenol

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Overview

What is Dry Socket?

Dry Socket Paste is formulated relieve the symptoms of alveolar osteitis ("dry socket syndrome"). Dry Socket Paste contains 4% guaicol and 4% eugenol in a petrolatum base.



What does Dry Socket look like?



What are the available doses of Dry Socket?

Sorry No records found.

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

Sorry No records found

How should I use Dry Socket?

Indicated for the relief of symptoms associated with post-extraction alveolar osteitis ("dry socket syndrome").

Establish a diagnosis of alveolar osteitis; typically characterized as a constant dull or throbbing ache, exacerbated by touch, approximately 2 days post extraction. The socket will have no clot present and will usually be packed with food debris.

Thoroughly rinse and de-bride the socket.

Introduce Dry Socket Paste into the socket using a flat-bladed instrument or a disposable syringe.

Tamp down the Dry Socket Paste, ensuring coverage of all exposed bone.

Do not cover the Dry Socket Paste.

Dry Socket Paste will remain in the extraction socket 3 to 5 days and will gradually wash out as the socket heals – there is no need for a separate visit to remove the product.


What interacts with Dry Socket?

Sorry No Records found


What are the warnings of Dry Socket?

Sorry No Records found


What are the precautions of Dry Socket?

Sorry No Records found


What are the side effects of Dry Socket?

Sorry No records found


What should I look out for while using Dry Socket?

This product should not be used with individuals with known sensitivities to guaicol or eugenol. This product should not be used with individuals who are pregnant or suspected to be pregnant without a prior physician consultation.

Do not swallow. Keep out of reach of children. For professional dental use only.


What might happen if I take too much Dry Socket?

Sorry No Records found


How should I store and handle Dry Socket?

Sorry No Records found


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Clinical Information

Chemical Structure

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Clinical Pharmacology

Non-Clinical Toxicology
This product should not be used with individuals with known sensitivities to guaicol or eugenol. This product should not be used with individuals who are pregnant or suspected to be pregnant without a prior physician consultation.

Do not swallow. Keep out of reach of children. For professional dental use only.

Heparin preparations containing sodium bisulfite reduce the absorption peak of Indocyanine Green in blood and, therefore, should not be used as an anticoagulant for the collection of samples for analysis.

For professional dental use only. Use only as directed. Not for unsupervised home use.

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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

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Interactions

Interactions

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