What is NDC 69367-245?

69367-245 is the product NDC for Sodium Sulfacetamide and Sulfur, Sulfacetamide sodium 80 mg/mL; Sulfur 40 mg/mL suspension, listed with the FDA by Westminster Pharmaceuticals, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

Westminster Pharmaceuticals, LLC, NDC labeler code 69367. 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 Sulfur?

14 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Sodium Sulfacetamide and Sulfur NDC 69367-245

NDC codes

FDA NDC Directory

Product NDC (as listed)69367-245Labeler and product segments. Claims need a package NDC.

Product NDC at billing width69367-0245Add 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
69367-245-16	6936702451669367024516	473 mL in 1 BOTTLE (69367-245-16)Marketed from Jun 18, 2021

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 Sulfur
Generic name (nonproprietary): sodium sulfacetamide and sulfur
Active ingredients: Sulfacetamide sodium — 80 mg/mLSulfur — 40 mg/mL
Dosage form: Suspension
Route: Topical
Labeler: Westminster Pharmaceuticals, LLCNDC labeler code 69367
Product type: Prescription drug
Marketing category: Unapproved drug (other)
Marketing start: Jun 18, 2021
Listing expires: Dec 31, 2026
Other FDA classes: Sulfonamides (Chemical structure)
Identifiers: Product ID 69367-245_b4e89e57-397a-4578-bc59-709cb46db033SPL ID b4e89e57-397a-4578-bc59-709cb46db033SPL set ID e9b60d3f-3f3f-477d-92d7-fe0ba07e21deRxCUI 1010234UNII 4NRT660KJQ, 70FD1KFU70
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

N469367024516 followed by a unit qualifier and the quantity

Package 69367-0245-16. 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 Apr 29, 2025.

Indications (excerpt from the label)

INDICATIONS Sodium Sulfacetamide 8% and Sulfur 4% Topical Suspension 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)

About NDC 69367-245

What is NDC 69367-245?: 69367-245 is the product NDC for Sodium Sulfacetamide and Sulfur, Sulfacetamide sodium 80 mg/mL; Sulfur 40 mg/mL suspension, listed with the FDA by Westminster Pharmaceuticals, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Sodium Sulfacetamide and Sulfur.
What is the active ingredient?: Sulfacetamide sodium, Sulfur.
Who is the labeler?: Westminster Pharmaceuticals, LLC, NDC labeler code 69367. 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 Sulfur?: 14 other product NDCs are listed under this name. See all Sodium Sulfacetamide and Sulfur NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Sodium Sulfacetamide and Sulfur NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Sodium Sulfacetamide And Sulfursulfacetamide sodium, sulfur	Sulfacetamide sodium 80 mg/mL; Sulfur 40 mg/mL	SuspensionTopical	BioComp Pharma, Inc.	44523-624	44523-0624-16
Sodium Sulfacetamide And Sulfursulfacetamide sodium, sulfur	Sulfacetamide sodium 98 mg/g; Sulfur 48 mg/g	LotionTopical	BioComp Pharma, Inc.	44523-600	44523-0600-02
Sodium Sulfacetamide And Sulfursodium sulfacetamide 9.8% and sulfur 4.8%	Sulfacetamide sodium 98 mg/g; Sulfur 48 mg/g	EmulsionTopical	BioComp Pharma, Inc.	44523-748	44523-0748-10
Sodium Sulfacetamide and Sulfursulfacetamide sodium, sulfur	Sulfacetamide sodium 100 mg/g; Sulfur 50 mg/g	LiquidTopical	Method Pharmaceuticals, LLC	58657-472	58657-0472-0658657-0472-0758657-0472-08+2 more
Sodium Sulfacetamide and Sulfursulfacetamide sodium, sulfur	Sulfacetamide sodium 100 mg/g; Sulfur 50 mg/g	LiquidTopical	Bryant Ranch Prepack	63629-9259	63629-9259-01
Sodium Sulfacetamide and Sulfursulfacetamide sodium, sulfur	Sulfacetamide sodium 100 mg/g; Sulfur 50 mg/g	LiquidTopical	Bryant Ranch Prepack	63629-9260	63629-9260-01
Sodium Sulfacetamide and Sulfursulfacetamide sodium, sulfur	Sulfacetamide sodium 100 mg/g; Sulfur 50 mg/g	LiquidTopical	Bryant Ranch Prepack	63629-9261	63629-9261-01
Sodium Sulfacetamide and Sulfursulfacetamide sodium, sulfur	Sulfacetamide sodium 100 mg/g; Sulfur 50 mg/g	LiquidTopical	Bryant Ranch Prepack	71335-2940	71335-2940-01
Sodium Sulfacetamide and Sulfursulfacetamide sodium, sulfur	Sulfacetamide sodium 100 mg/g; Sulfur 50 mg/g	LiquidTopical	Bryant Ranch Prepack	72162-1664	72162-1664-0272162-1664-0472162-1664-07
Sodium Sulfacetamide And Sulfursulfacetamide sodium, sulfur	Sulfacetamide sodium 100 mg/g; Sulfur 50 mg/g	LotionTopical	BioComp Pharma, Inc.	44523-607	44523-0607-0144523-0607-02

All 15 Sodium Sulfacetamide and Sulfur NDCs