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Sumaxin

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Overview

What is Sumaxin?

DESCRIPTION: Sodium sulfacetamide is a sulfacetamide with antibacterial activity while sulfur acts as a keratolytic agent. Chemically sodium sulfacetamide is N-[(4-aminophenyl) sulfonyl]-acetamide, monosodium salt, monohydrate. Each mL of Sumaxin (sodium sulfacetamide 9% and sulfur 4%) Wash contains 90mg of sodium sulfacetamide and 40 mg of sulfur in a formulation consisting of: aloe, butylated hydroxytoluene, cetyl alcohol, disodium oleamido MEA sulfosuccinate, edetate disodium, fragrance, glyceryl stearate/PEG-100 stearate, green tea, magnesium aluminum silicate, methylparaben, propylparaben, purified water, sodium cocoyl isethionate, sodium methyl cocoyl taurate, sodium thiosulfate, stearyl alcohol, xanthan gum.



What does Sumaxin look like?



What are the available doses of Sumaxin?

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

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How should I use Sumaxin?

INDICATIONS: Sumaxin (sodium sulfacetamide 9% and sulfur 4%) Wash is indicated for the topical control of acne vulgaris, acne rosacea and seborrheic dermatitis.

DOSAGE AND ADMINISTRATION: Apply Sumaxin (sodium sulfacetamide 9% and sulfur 4%) Wash once or twice daily to affected areas, or as directed by your physician.  Wet skin and liberally apply to areas to be cleansed. Massage  gently  into skin  for 10-20 seconds,, working into a full lather, rinse thoroughly and pat dry. If  drying  occurs, it may be controlled by rinsing off Sumaxin (sodium sulfacetamide 9% and sulfur 4%)  Wash  sooner or using less often.


What interacts with Sumaxin?

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What are the warnings of Sumaxin?

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What are the precautions of Sumaxin?

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What are the side effects of Sumaxin?

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What should I look out for while using Sumaxin?

CONTRAINDICATIONS: Sumaxin (sodium sulfacetamide 9% and sulfur 4%) Wash are contraindicated for use by patients having known hypersensitivity to sulfonamides, sulfur or any other component of this preparation. Sumaxin (sodium sulfacetamide 9% and sulfur 4%) Wash is not to be used by patients with kidney disease.

WARNINGS: Although rare, sensitivity to sodium sulfacetamide may occur. Therefore, caution and careful supervision should be observed when prescribing this drug for patients who may be prone to hypersensitivity to topical sulfonamides. Systemic toxic reactions such as agranulocytosis, acute hemolytic anemia, purpura hemorrhagica, drug fever, jaundice, and contact dermatitis indicate hypersensitivity to sulfonamides. Particular caution should be employed if areas of denuded or abraded skin are involved.


What might happen if I take too much Sumaxin?

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How should I store and handle Sumaxin?

Store at controlled room temperature 20°-25°C (68°-77°F); excursions permitted to 15°-30°C (59°-86°F). Please refer to current USP.Dispense in tight, light-resistant containers as defined in USP/NF with a child-resistant closure.KEEP OUT OF REACH OF CHILDRENStore at controlled room temperature 20°-25°C (68°-77°F); excursions permitted to 15°-30°C (59°-86°F). Please refer to current USP.Dispense in tight, light-resistant containers as defined in USP/NF with a child-resistant closure.KEEP OUT OF REACH OF CHILDRENStore at controlled room temperature 20°-25°C (68°-77°F); excursions permitted to 15°-30°C (59°-86°F). Please refer to current USP.Dispense in tight, light-resistant containers as defined in USP/NF with a child-resistant closure.KEEP OUT OF REACH OF CHILDRENHOW SUPPLIED: Sumaxin (sodium sulfacetamide 9% and sulfur 4%) Wash is availible in 16oz. bottle, NDC 43538-130-16.Store at controlled room temperature 15°-30°C (59°-86°F). Protect from freezing.KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.HOW SUPPLIED: Sumaxin (sodium sulfacetamide 9% and sulfur 4%) Wash is availible in 16oz. bottle, NDC 43538-130-16.Store at controlled room temperature 15°-30°C (59°-86°F). Protect from freezing.KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.HOW SUPPLIED: Sumaxin (sodium sulfacetamide 9% and sulfur 4%) Wash is availible in 16oz. bottle, NDC 43538-130-16.Store at controlled room temperature 15°-30°C (59°-86°F). Protect from freezing.KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.


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Clinical Information

Chemical Structure

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Clinical Pharmacology

Non-Clinical Toxicology
CONTRAINDICATIONS: Sumaxin (sodium sulfacetamide 9% and sulfur 4%) Wash are contraindicated for use by patients having known hypersensitivity to sulfonamides, sulfur or any other component of this preparation. Sumaxin (sodium sulfacetamide 9% and sulfur 4%) Wash is not to be used by patients with kidney disease.

WARNINGS: Although rare, sensitivity to sodium sulfacetamide may occur. Therefore, caution and careful supervision should be observed when prescribing this drug for patients who may be prone to hypersensitivity to topical sulfonamides. Systemic toxic reactions such as agranulocytosis, acute hemolytic anemia, purpura hemorrhagica, drug fever, jaundice, and contact dermatitis indicate hypersensitivity to sulfonamides. Particular caution should be employed if areas of denuded or abraded skin are involved.

Additive adverse effects resulting from cholinergic blockade may occur when hyoscyamine sulfate is administered concomitantly with other antimuscarinics, amantadine, haloperidol, phenothiazines, monoamine oxidase (MAO) inhibitors, tricyclic antidepressants or some antihistamines.

Antacids may interfere with the absorption of hyoscyamine sulfate. Administer hyoscyamine sulfate before meals; antacids after meals.

PRECAUTIONS: General - If irritation develops, use of the product should be discontinued and approriate therapy instituted. Patients should  be carefully observed for possible local irritation or sensitization during long-term therapy. The  object of this therapy is to achieve desquamation without irritation, but sodium sulfacetamide and sulfur can cause reddening and  scaling  of the  epidermis. These side effects are not unusual in  the treatment  of acne  vulgaris, but patients should be cautioned about the possibility.

Information for patients - Avoid contact with eyes, eyelids, lips and mucous membranes. If accidental contact occurs, rinse with water. If excessive irritation develops, discontinue use and consult your physician.

ADVERSE REACTIONS: Although rare, sodium sulfacetamide may cause local irritation.

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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

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).