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Sodium Sulfacetamide and Sulfer Emulsion

Generic: Sodium Sulfacetamide and Sulfer

Verified·Apr 23, 2026
NDC
73352-750
RxCUI
999604
Route
TOPICAL
ICD-10 indication
L70.0

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About Sodium Sulfacetamide and Sulfer Emulsion

What is this medication? Sodium sulfacetamide and sulfur emulsion is a topical prescription treatment used to manage several common inflammatory skin conditions. It is primarily indicated for the treatment of acne vulgaris, acne rosacea, and seborrheic dermatitis. This medication works through a dual-action approach involving its two active ingredients. Sodium sulfacetamide functions as an antibacterial agent by inhibiting the growth of bacteria on the skin surface, while sulfur acts as a keratolytic agent that helps to soften and shed the outermost layer of skin cells, preventing clogged pores and reducing flakiness. In addition to its antibacterial properties, this emulsion helps to reduce the redness, scaling, and formation of skin lesions associated with oily or irritated skin. It is frequently prescribed for patients who need a medical-grade solution to address persistent breakouts or the flushing and bumps associated with rosacea. Because the medication contains a sulfonamide, it is important for patients to inform their healthcare provider of any known allergies to sulfa drugs before starting treatment. The emulsion is applied directly to the affected areas as directed by a physician to improve the overall appearance and health of the skin.

Copay & patient assistance

Detailed copay and financial assistance information is not publicly available for this medication at this time. Please consult your pharmacist or the manufacturer's official patient support program for more details.

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Prescribing information

From the FDA-approved label for Sodium Sulfacetamide and Sulfer Emulsion. Official source: DailyMed (NLM) · Label effective Oct 15, 2025

Indications and usage
INDICATIONS Sodium Sulfacetamide 10% - Sulfur 1% Emulsion is indicated in the topical control of acne vulgaris, acne rosacea and seborrheic dermatitis.
Dosage and administration
DOSAGE AND ADMINISTRATION Apply Sodium Sulfacetamide 10% and Sulfur 1% Emulsion 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 Sodium Sulfacetamide 10% and Sulfur 1% Emulsion sooner or using less often.
Contraindications
CONTRAINDICATIONS Sodium Sulfacetamide 10% and Sulfur 1% Emulsion is contraindicated for use by patients having known hypersensitivity to sulfonamides, sulfur or any other component of this preparation. Sodium Sulfacetamide 10% and Sulfer 1% Emulsion is not to be used by patietns with kidney disease.
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. FOR EXTERNAL USE ONLY . Keep away from eyes. Keep out of reach of children. In case of accidental ingestion contact a poison control center immediately. Keep container tightly closed.
Adverse reactions
ADVERSE REACTIONS Although rare, sodium sulfacetamide may cause local irritation. Call your doctor for medical advice about side effects. To report a serious adverse event, please contact Trifluent Pharma, LLC at 1-888-927-5191.
Use in pregnancy
PREGNANCY - Category C Animal reproduction studies have not been conducted with Sodium Sulfacetamide 10% and Sulfer 1% Emulsion. It is not known whether Sodium Sulfacetamide 10% and Sulfer 1% Emulsion can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Sodium Silfacetamide 10% and Sulfer 1% Emulsion should be given to a pregnant woman only if clearly needed.

Label text is reproduced as-is from the FDA-approved label. We do not paraphrase, summarize, or omit. Content above is for informational purposes only and is not medical advice. Always consult your prescribing clinician or pharmacist before making decisions about your medication.

Conditions we've indexed resources for

Click a condition to see copay cards, grants, and PA rules specific to it. For the full list of FDA-approved indications, see Prescribing information above.

Prior authorization & coverage

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How this page is sourced

  • Drug identity verified against openFDA NDC Directory.
  • Label text (when shown) originates from NLM DailyMed.
  • Copay and assistance URLs verified periodically; if you hit a broken link, tell us.