NDC codes

FDA NDC Directory
Product NDC (as listed)72162-2250Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72162-2250Add 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
72162-2250-27216222500272162225002454 g in 1 BOTTLE, PLASTIC (72162-2250-2)Marketed from Mar 19, 2026

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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)
sulfacetamide sodium, sulfur
Active ingredients
Sulfacetamide sodium — 90 mg/gSulfur — 45 mg/g
Dosage form
Liquid
Route
Topical
Labeler
Bryant Ranch PrepackNDC labeler code 72162
Product type
Prescription drug
Marketing category
Unapproved drug (other)
Marketing start
Listing expires
Other FDA classes
Sulfonamides (Chemical structure)
Identifiers
Product ID 72162-2250_90ad47f3-5268-40ff-9cdd-b0a9aa527cb5SPL ID 90ad47f3-5268-40ff-9cdd-b0a9aa527cb5SPL set ID 25516616-2249-4b4f-be31-1a4378d03861RxCUI 1115894UNII 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

N472162225002 followed by a unit qualifier and the quantity

Package 72162-2250-02. 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 .

Indications (excerpt from the label)

INDICATIONS SODIUM SULFACETAMIDE 9% - SULFUR 4.5% CLEANSER is indicated for use 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 72162-2250

What is NDC 72162-2250?
72162-2250 is the product NDC for Sodium Sulfacetamide 9% and Sulfur 4.5% Cleanser, Sulfacetamide sodium 90 mg/g; Sulfur 45 mg/g liquid, listed with the FDA by Bryant Ranch Prepack. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Sodium Sulfacetamide 9% and Sulfur 4.5% Cleanser (Sulfacetamide sodium, Sulfur).
What is the active ingredient?
Sulfacetamide sodium, Sulfur.
Who is the labeler?
Bryant Ranch Prepack, NDC labeler code 72162. 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 9% and Sulfur 4.5% Cleanser?
1 other product NDC are listed under this name. See all Sodium Sulfacetamide 9% and Sulfur 4.5% 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 9% and Sulfur 4.5% Cleanser NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Sodium Sulfacetamide 9% and Sulfur 4.5% Cleansersulfacetamide sodium, sulfurSulfacetamide sodium 90 mg/g; Sulfur 45 mg/gLiquidTopicalMethod Pharmaceuticals58657-47458657-0474-16

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