Sodium Sulfacetamide, Sulfur NDC 42192-149

NDC codes

FDA NDC Directory

Product NDC (as listed)42192-149Labeler and product segments. Claims need a package NDC.

Product NDC at billing width42192-0149Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
42192-149-02	42192014902	57 g in 1 TUBE (42192-149-02)Marketed from Aug 14, 2014

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, Sulfur
Generic name (nonproprietary): sodium sulfacetamide and sulfur
Active ingredients: Sulfacetamide sodium — 100 mg/gSulfur — 50 mg/g
Dosage form: Cream
Route: Topical
Labeler: Acella Pharmaceuticals, LLC
Product type: Prescription drug
Marketing category: Unapproved drug (other)
Marketing start: Aug 14, 2014
Listing expires: Dec 31, 2027
Other FDA classes: Sulfonamides (Chemical structure)
Identifiers: Product ID 42192-149_568031c9-929d-3ead-e063-6394a90a64a3SPL ID 568031c9-929d-3ead-e063-6394a90a64a3SPL set ID 99705c54-b7af-423d-8f20-881e8fea236fRxCUI 1005834UNII 70FD1KFU70, 4NRT660KJQ
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

N442192014902 followed by a unit qualifier and the quantity

Package 42192-0149-02. 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 Jul 13, 2026.

Indications (excerpt from the label)

INDICATIONS: Sodium Sulfacetamide 10% Sulfur 5% Emollient Cream is indicated in the topical control of acne vulgaris, acne rosacea and seborrheic dermatitis.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)