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TRETINOIN, HYDROCORTISONE

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Overview

What is DR. THROWERS HYDROTET?



What does DR. THROWERS HYDROTET look like?



What are the available doses of DR. THROWERS HYDROTET?

Sorry No records found.

What should I talk to my health care provider before I take DR. THROWERS HYDROTET?

Sorry No records found

How should I use DR. THROWERS HYDROTET?

RX STRENGTH TOPICAL RETINOID FOR TREATMENT OF ACNE, SHAVING BUMPS, AND SPECIFIC BUMPY SKIN PROBLEMS. LEAVES SKIN SMOOTH, CLEAR AND NEW.

uSES: ACNE AND SPECIFIC SKIN CONDITIONS.

APPLY MEDICATION TO OILY AREA ONLY OF THE FACE IN VERY THIN LAYER. LEAVE ON OVERNIGHT.


What interacts with DR. THROWERS HYDROTET?

Sorry No Records found


What are the warnings of DR. THROWERS HYDROTET?

Amoxicillin and Clavulanate Potassium for Oral Suspension 600 mg/42.9 mg per 5 mL should be used with caution in patients with evidence of hepatic dysfunction. Hepatic toxicity associated with the use of amoxicillin/clavulanate potassium is usually reversible. On rare occasions, deaths have been reported (less than 1 death reported per estimated 4 million prescriptions worldwide). These have generally been cases associated with serious underlying diseases or concomitant medications. (See and .)


What are the precautions of DR. THROWERS HYDROTET?

Sorry No Records found


What are the side effects of DR. THROWERS HYDROTET?

Sorry No records found


What should I look out for while using DR. THROWERS HYDROTET?

STOP USE IF SKIN BECOMES IRRITATED (PINK, RED DARKER, OR EXCESSIVE PEELING). cONTACT DR. THROWER FOR INSTRUCTIONS. FOR EXTERNAL USE ONLY. KEEP OUT OF REACH OF CHILDREN. FEDERAL LAW PROHIBITS THE TRANSFER OF THIS DRUG TO ANY OTHER PERSON OTHER THAN FOR WHOM IT IS PRESCRIBED.


What might happen if I take too much DR. THROWERS HYDROTET?

Sorry No Records found


How should I store and handle DR. THROWERS HYDROTET?

Sorry No Records found


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Clinical Information

Chemical Structure

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Clinical Pharmacology

Non-Clinical Toxicology
STOP USE IF SKIN BECOMES IRRITATED (PINK, RED DARKER, OR EXCESSIVE PEELING). cONTACT DR. THROWER FOR INSTRUCTIONS. FOR EXTERNAL USE ONLY. KEEP OUT OF REACH OF CHILDREN. FEDERAL LAW PROHIBITS THE TRANSFER OF THIS DRUG TO ANY OTHER PERSON OTHER THAN FOR WHOM IT IS PRESCRIBED.

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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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Review

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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

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).