NDC codes

FDA NDC Directory
Product NDC (as listed)72162-2246Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72162-2246Add 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
72162-2246-2721622246027216222460228 g in 1 BOTTLE, PLASTIC (72162-2246-2)Marketed from May 15, 2022
72162-2246-4721622246047216222460457 g in 1 BOTTLE, PLASTIC (72162-2246-4)Marketed from May 15, 2022

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)
sodium sulfacetamide 10% and sulfur 5% emollient cream
Active ingredients
Sulfacetamide sodium — 100 mg/gSulfur — 50 mg/g
Dosage form
Cream
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 72162-2246_19d9af58-ede2-4536-879e-a934ae957c2fSPL ID 19d9af58-ede2-4536-879e-a934ae957c2fSPL set ID 4ebfcaae-a375-45aa-a7f9-2b622f564f02RxCUI 1005834UNII 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

N472162224602 followed by a unit qualifier and the quantity

Package 72162-2246-02. 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: This product 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 72162-2246

What is NDC 72162-2246?
72162-2246 is the product NDC for SODIUM SULFACETAMIDE 10% AND SULFUR 5% Emollient Cream, Sulfacetamide sodium 100 mg/g; Sulfur 50 mg/g cream, listed with the FDA by Bryant Ranch Prepack. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
SODIUM SULFACETAMIDE 10% AND SULFUR 5% Emollient Cream.
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 10% AND SULFUR 5% Emollient Cream?
1 other product NDC are listed under this name. See all SODIUM SULFACETAMIDE 10% AND SULFUR 5% Emollient Cream 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 5% Emollient Cream NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
SODIUM SULFACETAMIDE 10% AND SULFUR 5% Emollient CreamSulfacetamide sodium 100 mg/g; Sulfur 50 mg/gCreamTopicalMethod Pharmaceuticals, LLC58657-46858657-0468-0158657-0468-02

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