
SULFACETAMIDE SODIUM / SULFUR CREAM 10% / 2% 57 GM
Generic: Sulfacetamide Sodium and Sulfur
SULFACETAMIDE SODIUM / SULFUR CREAM 10% / 2% 57 GM
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Identification
Sulfacetamide Sodium and Sulfur
Sodium Sulfacetamide 10 Sulfur 2 cream
Acella Pharmaceuticals, LLC
HUMAN PRESCRIPTION DRUG
Administration
CREAM
TOPICAL
Active Ingredients
| Ingredient | Strength |
|---|---|
| SULFACETAMIDE SODIUM | 100 mg/g |
| SULFUR | 20 mg/g |
Pharmacological Class
Data sourced from openFDA / DailyMed. For full prescribing information, consult the drug label.
Wholesale compliance resources
Clinical Drug Information
Indications & Usage
INDICATIONS: Sodium Sulfacetamide 10% Sulfur 2% Cream is indicated in the topical control of acne vulgaris, acne rosacea and seborrheic dermatitis.
Warnings
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.
Dosage & Administration
DOSAGE AND ADMINISTRATION: Cleanse skin thoroughly before application. Apply a thin layer to affected areas 1-3 times daily or as directed by a physician. To minimize potential dryness, start with one application daily, then gradually increase to 2-3 times daily as needed or as directed by a physician.
Adverse Reactions
ADVERSE REACTIONS: Although rare, sodium sulfacetamide may cause local irritation.
Information for Patients
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.
Clinical data sourced from openFDA drug labeling. For complete prescribing information, consult the full drug label.