Prescription drug · UNAPPROVED DRUG OTHER
Sodium Sulfacetamide and Sulfer Emulsion (Sodium sulfacetamide and sulfer) NDC 73352-750
Sulfacetamide sodium 100 mg/mL; Sulfur 10 mg/mL · Emulsion · Topical · Trifluent Pharma
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 73352-750-01 | 7335207500173352075001 | 177 mL in 1 BOTTLE (73352-750-01)Marketed from Oct 4, 2025 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Sodium Sulfacetamide and Sulfer Emulsion
- Generic name (nonproprietary)
- sodium sulfacetamide and sulfer
- Active ingredients
- Sulfacetamide sodium — 100 mg/mLSulfur — 10 mg/mL
- Dosage form
- Emulsion
- Route
- Topical
- Labeler
- Trifluent PharmaNDC labeler code 73352
- Product type
- Prescription drug
- Marketing category
- Unapproved drug (other)
- Marketing start
- Listing expires
- Other FDA classes
- Sulfonamides (Chemical structure)
- Identifiers
- Product ID 73352-750_41396a22-cc34-94f2-e063-6294a90afb65SPL ID 41396a22-cc34-94f2-e063-6294a90afb65SPL set ID 40601d03-aea0-b0a6-e063-6394a90a1698RxCUI 999604UNII 4NRT660KJQ, 70FD1KFU70UPC 0373352750016
- Pharmacologic class
- Sulfonamide Antibacterial
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Topical products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N473352075001followed by a unit qualifier and the quantityPackage 73352-0750-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
INDICATIONS Sodium Sulfacetamide 10% - Sulfur 1% Emulsion is indicated in the topical control of acne vulgaris, acne rosacea and seborrheic dermatitis.
Excerpt only. Read the full label for complete information.
About NDC 73352-750
- What is NDC 73352-750?
- 73352-750 is the product NDC for Sodium Sulfacetamide and Sulfer Emulsion, Sulfacetamide sodium 100 mg/mL; Sulfur 10 mg/mL emulsion, listed with the FDA by Trifluent Pharma. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Sodium Sulfacetamide and Sulfer Emulsion (Sodium Sulfacetamide and Sulfer).
- What is the active ingredient?
- Sulfacetamide sodium, Sulfur.
- Who is the labeler?
- Trifluent Pharma, NDC labeler code 73352. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Sodium Sulfacetamide and Sulfer Emulsion?
- None: this is the only finished product listed under this name.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.