NDC codes

FDA NDC Directory
Product NDC (as listed)50405-851Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50405-0851Add 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 NDC11-digit (billing)PackageCopy
50405-851-015040508510150405085101227 g in 1 BOTTLE (50405-851-01)Marketed from May 3, 2023

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

Generic name (nonproprietary)
sodium sulfacetamide and sulfur
Active ingredients
Sulfacetamide sodium — 100 mg/gSulfur — 20 mg/g
Dosage form
Lotion
Route
Topical
Labeler
SOHM, IncNDC labeler code 50405
Product type
Prescription drug
Marketing category
Unapproved drug (other)
Marketing start
Listing expires
Other FDA classes
Sulfonamides (Chemical structure)
Identifiers
Product ID 50405-851_67acba09-6267-4139-ad2b-e6b7849752a9SPL ID 67acba09-6267-4139-ad2b-e6b7849752a9SPL set ID 480b4c92-45a1-4ac8-83ee-791abf1b8759RxCUI 1000895UNII 4NRT660KJQ, 70FD1KFU70UPC 0342582600231
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

N450405085101 followed by a unit qualifier and the quantity

Package 50405-0851-01. 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: Sulfacetamide Sodium and Sulfur Cleanser 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 50405-851

What is NDC 50405-851?
50405-851 is the product NDC for Sodium Sulfacetamide 10 % and Sulfur 2 % Cleanser, Sulfacetamide sodium 100 mg/g; Sulfur 20 mg/g lotion, listed with the FDA by SOHM, Inc. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Sodium Sulfacetamide 10 % and Sulfur 2 % Cleanser (Sodium Sulfacetamide and Sulfur).
What is the active ingredient?
Sulfacetamide sodium, Sulfur.
Who is the labeler?
SOHM, Inc, NDC labeler code 50405. 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 10 % and Sulfur 2 % Cleanser?
3 other product NDCs are listed under this name. See all Sodium Sulfacetamide 10 % and Sulfur 2 % Cleanser 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 10 % and Sulfur 2 % Cleanser NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Sodium Sulfacetamide 10% and Sulfur 2% Cleansersulfacetamide sodium, sulfurSulfacetamide sodium 100 mg/g; Sulfur 20 mg/gLiquidTopicalAkron Pharma Inc.71399-048571399-0485-08
Sodium Sulfacetamide 10% and Sulfur 2% Cleansersulfacetamide sodium, sulfurSulfacetamide sodium 100 mg/g; Sulfur 20 mg/gLiquidTopicalMethod Pharmaceuticals58657-47158657-0471-08
Sodium Sulfacetamide 10% and Sulfur 2% Cleansersulfacetamide sodium, sulfurSulfacetamide sodium 100 mg/g; Sulfur 20 mg/gLiquidTopicalBryant Ranch Prepack72162-224872162-2248-02

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