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Phenolsulfonic Acid and Sulfuric Acid

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Overview

What is DEBACTEROL Canker Sore Pain Relief?

Debacterol is a dark brown, semi-viscous liquid. It contains sulfonated phenolics and sulfuric acid, which are tissue denaturants, in an aqueous solution.



What does DEBACTEROL Canker Sore Pain Relief look like?



What are the available doses of DEBACTEROL Canker Sore Pain Relief?

Contains 50% Sulfonated phenolics and 30% sulfuric acid in an aqueous solution.

What should I talk to my health care provider before I take DEBACTEROL Canker Sore Pain Relief?

Sorry No records found

How should I use DEBACTEROL Canker Sore Pain Relief?

Debacterol is indicated in the topical treatment of ulcerating lesions of the oral cavity such as Recurrent Aphthous Stomatitis (Canker Sores). Debacterol provides relief from the pain and discomfort of oral mucosal ulcers. .


What interacts with DEBACTEROL Canker Sore Pain Relief?

Sorry No Records found


What are the warnings of DEBACTEROL Canker Sore Pain Relief?

Sorry No Records found


What are the precautions of DEBACTEROL Canker Sore Pain Relief?

Sorry No Records found


What are the side effects of DEBACTEROL Canker Sore Pain Relief?

Sorry No records found


What should I look out for while using DEBACTEROL Canker Sore Pain Relief?

Keep out of reach of children. Do not use if allergic to a material that contains sulfur in any form. Because of its nature, prolonged use of Debacterol on normal tissue should be avoided. Debacterol will eventually necrotize and slough all tissue to which it is applied sufficient volume and should be applied carefully. Debacterol may be harmful with swallowed. If ingested do not induce vomiting. Immediately get medical help or contact a Poison Control Center. If eye exposure occurs, immediately remove any contact lenses and irrigate eyes for at least 15 minutes with lukewarm water and contact a physician.


What might happen if I take too much DEBACTEROL Canker Sore Pain Relief?

Sorry No Records found


How should I store and handle DEBACTEROL Canker Sore Pain Relief?

Store reconstituted suspension under refrigeration. Discard unused suspension after 10 days. Store dry powder for oral suspension at 20°–25°C (68°–77°F). See USP controlled room temperature. Dispense in original container.Swab contains 0.2 ml of product. (NDC-62942-101-02)Vial contains 1.5 ml of product. (NDC-62942-101-03)Swab contains 0.2 ml of product. (NDC-62942-101-02)Vial contains 1.5 ml of product. (NDC-62942-101-03)


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Clinical Information

Chemical Structure

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Clinical Pharmacology

Non-Clinical Toxicology
Keep out of reach of children. Do not use if allergic to a material that contains sulfur in any form. Because of its nature, prolonged use of Debacterol on normal tissue should be avoided. Debacterol will eventually necrotize and slough all tissue to which it is applied sufficient volume and should be applied carefully. Debacterol may be harmful with swallowed. If ingested do not induce vomiting. Immediately get medical help or contact a Poison Control Center. If eye exposure occurs, immediately remove any contact lenses and irrigate eyes for at least 15 minutes with lukewarm water and contact a physician.

Debacterol is for use in the oral cavity only. Avoid eye contact. Saftey and effectiveness in pregnant women and children under the age of 12 has not been established.

Debacterol may cause local irritation upon administration. If excess irritation occurs during use, a rinse with sodium bicarbonate (baking soda) solution will neutralize the reaction (use 0.5 teaspoon in 120ml of water). If condition persists contact a health care professional.

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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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