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sodium sulfacetamide, sulfer

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Overview

What is Rosanil?

Sodium sulfacetamide is a sulfonamide with antibacterial activity while sulfur acts as a keratolytic agent. Chemically sodium sulfacetamide is N-[(4-aminophenyl)sulfonyl]-acetamide, monosodium salt, monohydrate. The structural formula is:

Each gram of ROSANIL (sodium sulfacetamide 10% and sulfur 5%) Cleanser contains: sodium sulfacetamide 10% (100 mg), sulfur 5% (50 mg). butylated hydroxytoluene, edetate disodium, emulsifying wax, hydrochloric acid, light mineral oil, methylparaben, PPG-2 hydroxyethyl coco/isostearamide, propylparaben, purified water, sodium cocoyl isethionate, sodium lauryl sulfoacetate (and) disodium laureth sulfosuccinate, and sodium thiosulfate.



What does Rosanil look like?



What are the available doses of Rosanil?

Sorry No records found.

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

Sorry No records found

How should I use Rosanil?

ROSANIL Cleanser is indicated in the topical control of acne vulgaris, acne rosacea and seborrheic dermatitis.

Wash affected areas once or twice daily, or as directed by your physician. Avoid contact with eyes or mucous membranes. 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 cleanser off sooner or using less often.


What interacts with Rosanil?

Sorry No Records found


What are the warnings of Rosanil?

Sorry No Records found


What are the precautions of Rosanil?

Sorry No Records found


What are the side effects of Rosanil?

Although rare, sodium sulfacetamide may cause local irritation.


What should I look out for while using Rosanil?

ROSANIL Cleanser is contraindicated for use by patients having known hypersensitivity to sulfonamides, sulfur or any other component of this preparation. ROSANIL Cleanser is not to be used by patients with kidney disease.

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.

FOR EXTERNAL USE ONLY.

Keep out of reach of children.


What might happen if I take too much Rosanil?

Sorry No Records found


How should I store and handle Rosanil?

Storage temperature should not exceed 30°C (86°F).Keep out of reach of children.Storage temperature should not exceed 30°C (86°F).Keep out of reach of children.ROSANIL (sodium sulfacetamide 10% and sulfur 5%) Cleanser is available in a 6 oz tube.NDCStore at controlled room temperature 20° - 25°C (68° - 77°F).Marketed by:GALDERMA LABORATORIES, L.P.Fort Worth, Texas 76177 USAManufactured by:DPT Laboratories, Ltd.San Antonio, Texas 78215 USAGALDERMA is a registered trademark. 325076-0706 Revised: July 2006ROSANIL (sodium sulfacetamide 10% and sulfur 5%) Cleanser is available in a 6 oz tube.NDCStore at controlled room temperature 20° - 25°C (68° - 77°F).Marketed by:GALDERMA LABORATORIES, L.P.Fort Worth, Texas 76177 USAManufactured by:DPT Laboratories, Ltd.San Antonio, Texas 78215 USAGALDERMA is a registered trademark. 325076-0706 Revised: July 2006ROSANIL (sodium sulfacetamide 10% and sulfur 5%) Cleanser is available in a 6 oz tube.NDCStore at controlled room temperature 20° - 25°C (68° - 77°F).Marketed by:GALDERMA LABORATORIES, L.P.Fort Worth, Texas 76177 USAManufactured by:DPT Laboratories, Ltd.San Antonio, Texas 78215 USAGALDERMA is a registered trademark. 325076-0706 Revised: July 2006ROSANIL (sodium sulfacetamide 10% and sulfur 5%) Cleanser is available in a 6 oz tube.NDCStore at controlled room temperature 20° - 25°C (68° - 77°F).Marketed by:GALDERMA LABORATORIES, L.P.Fort Worth, Texas 76177 USAManufactured by:DPT Laboratories, Ltd.San Antonio, Texas 78215 USAGALDERMA is a registered trademark. 325076-0706 Revised: July 2006


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Clinical Information

Chemical Structure

No Image found
Clinical Pharmacology

The most widely accepted mechanism of action of sulfonamides is the Woods-Fildes theory which is based on the fact that sulfonamides act as competitive antagonists to para-aminobenzoic acid (PABA), an essential component for bacterial growth. While absorption through intact skin has not been determined, sodium sulfacetamide is readily absorbed from the gastrointestinal tract when taken orally and excreted in the urine, largely unchanged. The biological half-life has variously been reported as 7 to 12.8 hours. The exact mode of action of sulfur in the treatment of acne is unknown, but it has been reported that it inhibits the growth of and the formation of free fatty acids.

Non-Clinical Toxicology
ROSANIL Cleanser is contraindicated for use by patients having known hypersensitivity to sulfonamides, sulfur or any other component of this preparation. ROSANIL Cleanser is not to be used by patients with kidney disease.

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.

FOR EXTERNAL USE ONLY.

Keep out of reach of children.

Although Levobunolol Hydrochloride Ophthalmic Solution used alone has little or no effect on pupil size, mydriasis resulting from concomitant therapy with Levobunolol Hydrochloride Ophthalmic Solution and epinephrine may occur.

Close observation of the patient is recommended when a beta-blocker is administered to patients receiving catecholamine-depleting drugs such as reserpine, because of possible additive effects and the production of hypotension and/or marked bradycardia, which may produce vertigo, syncope, or postural hypotension. Patients receiving beta-adrenergic blocking agents along with either oral or intravenous calcium antagonists should be monitored for possible atrioventricular conduction disturbances, left ventricular failure and hypotension. In patients with impaired cardiac function, simultaneous use should be avoided altogether. The concomitant use of beta-adrenergic blocking agents with digitalis and calcium antagonists may have additive effects on prolonging atrioventricular conduction time.

Phenothiazine-related compounds and beta-adrenergic blocking agents may have additive hypotensive effects due to the inhibition of each other's metabolism.

General:

Information for Patients:

Carcinogenesis, Mutagenesis and Impairment of Fertility:

Pregnancy:

Nursing Mothers:

Pediatric Use:

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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Interactions

Interactions

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